Please choose an event type to view the corresponding MedsFacts report:

INTERNATIONAL NORMALISED RATIO INCREASED ( 5217 FDA reports)
DRUG INTERACTION ( 2875 FDA reports)
DYSPNOEA ( 2567 FDA reports)
ATRIAL FIBRILLATION ( 2109 FDA reports)
NAUSEA ( 1940 FDA reports)
ANAEMIA ( 1859 FDA reports)
PAIN ( 1822 FDA reports)
DIZZINESS ( 1821 FDA reports)
ASTHENIA ( 1724 FDA reports)
FALL ( 1649 FDA reports)
FATIGUE ( 1566 FDA reports)
DIARRHOEA ( 1536 FDA reports)
HYPOTENSION ( 1483 FDA reports)
OEDEMA PERIPHERAL ( 1471 FDA reports)
PNEUMONIA ( 1456 FDA reports)
VOMITING ( 1400 FDA reports)
HAEMOGLOBIN DECREASED ( 1335 FDA reports)
HAEMORRHAGE ( 1267 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1263 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1213 FDA reports)
RENAL FAILURE ACUTE ( 1170 FDA reports)
DRUG INEFFECTIVE ( 1152 FDA reports)
PYREXIA ( 1148 FDA reports)
HEADACHE ( 1133 FDA reports)
ANXIETY ( 1124 FDA reports)
DEEP VEIN THROMBOSIS ( 1121 FDA reports)
CHEST PAIN ( 1090 FDA reports)
PULMONARY EMBOLISM ( 1052 FDA reports)
PAIN IN EXTREMITY ( 994 FDA reports)
MALAISE ( 975 FDA reports)
BACK PAIN ( 968 FDA reports)
ABDOMINAL PAIN ( 949 FDA reports)
CARDIAC FAILURE ( 916 FDA reports)
WEIGHT DECREASED ( 912 FDA reports)
ARTHRALGIA ( 896 FDA reports)
DEATH ( 880 FDA reports)
HYPERTENSION ( 874 FDA reports)
RENAL FAILURE ( 869 FDA reports)
CONFUSIONAL STATE ( 865 FDA reports)
CONDITION AGGRAVATED ( 852 FDA reports)
CEREBROVASCULAR ACCIDENT ( 839 FDA reports)
INJURY ( 809 FDA reports)
DECREASED APPETITE ( 785 FDA reports)
DEHYDRATION ( 777 FDA reports)
HAEMATURIA ( 768 FDA reports)
RASH ( 758 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 744 FDA reports)
COUGH ( 737 FDA reports)
PLEURAL EFFUSION ( 734 FDA reports)
MYOCARDIAL INFARCTION ( 712 FDA reports)
EPISTAXIS ( 692 FDA reports)
CONTUSION ( 683 FDA reports)
BLOOD CREATININE INCREASED ( 676 FDA reports)
SEPSIS ( 663 FDA reports)
URINARY TRACT INFECTION ( 633 FDA reports)
INSOMNIA ( 633 FDA reports)
DEPRESSION ( 631 FDA reports)
PROTHROMBIN TIME PROLONGED ( 629 FDA reports)
SYNCOPE ( 628 FDA reports)
THROMBOSIS ( 626 FDA reports)
GAIT DISTURBANCE ( 626 FDA reports)
BRADYCARDIA ( 622 FDA reports)
CONSTIPATION ( 614 FDA reports)
HAEMATOMA ( 606 FDA reports)
THROMBOCYTOPENIA ( 604 FDA reports)
CEREBRAL HAEMORRHAGE ( 601 FDA reports)
RESPIRATORY FAILURE ( 599 FDA reports)
LOSS OF CONSCIOUSNESS ( 585 FDA reports)
CARDIAC ARREST ( 574 FDA reports)
PRURITUS ( 559 FDA reports)
RECTAL HAEMORRHAGE ( 557 FDA reports)
HYPOAESTHESIA ( 540 FDA reports)
BLOOD GLUCOSE INCREASED ( 531 FDA reports)
COAGULOPATHY ( 531 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 530 FDA reports)
PARAESTHESIA ( 525 FDA reports)
HAEMATOCRIT DECREASED ( 517 FDA reports)
RENAL IMPAIRMENT ( 506 FDA reports)
BLOOD PRESSURE DECREASED ( 504 FDA reports)
PLATELET COUNT DECREASED ( 502 FDA reports)
ERYTHEMA ( 500 FDA reports)
MUSCULAR WEAKNESS ( 490 FDA reports)
OSTEONECROSIS OF JAW ( 482 FDA reports)
OSTEOARTHRITIS ( 472 FDA reports)
PALPITATIONS ( 472 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 466 FDA reports)
INFECTION ( 466 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 465 FDA reports)
SOMNOLENCE ( 464 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 462 FDA reports)
CONVULSION ( 462 FDA reports)
NEUROPATHY PERIPHERAL ( 460 FDA reports)
ABDOMINAL PAIN UPPER ( 459 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 459 FDA reports)
CARDIOMEGALY ( 458 FDA reports)
TACHYCARDIA ( 453 FDA reports)
CELLULITIS ( 452 FDA reports)
HAEMOPTYSIS ( 446 FDA reports)
ANHEDONIA ( 433 FDA reports)
PULMONARY HYPERTENSION ( 433 FDA reports)
DYSPHAGIA ( 432 FDA reports)
MELAENA ( 430 FDA reports)
MYALGIA ( 425 FDA reports)
VISION BLURRED ( 425 FDA reports)
WEIGHT INCREASED ( 420 FDA reports)
ECONOMIC PROBLEM ( 413 FDA reports)
ARRHYTHMIA ( 410 FDA reports)
MITRAL VALVE INCOMPETENCE ( 408 FDA reports)
MUSCLE SPASMS ( 408 FDA reports)
HYPERHIDROSIS ( 402 FDA reports)
HYPERKALAEMIA ( 401 FDA reports)
FLUSHING ( 399 FDA reports)
FEELING ABNORMAL ( 397 FDA reports)
BRONCHITIS ( 389 FDA reports)
MENTAL STATUS CHANGES ( 389 FDA reports)
HEART RATE INCREASED ( 387 FDA reports)
BLOOD UREA INCREASED ( 384 FDA reports)
SWELLING ( 382 FDA reports)
EMOTIONAL DISTRESS ( 379 FDA reports)
PANCYTOPENIA ( 374 FDA reports)
GASTRIC HAEMORRHAGE ( 373 FDA reports)
INTERSTITIAL LUNG DISEASE ( 368 FDA reports)
NEUTROPENIA ( 367 FDA reports)
HYPONATRAEMIA ( 365 FDA reports)
TREMOR ( 365 FDA reports)
VENTRICULAR TACHYCARDIA ( 363 FDA reports)
RENAL FAILURE CHRONIC ( 361 FDA reports)
ATELECTASIS ( 361 FDA reports)
OEDEMA ( 360 FDA reports)
CORONARY ARTERY DISEASE ( 354 FDA reports)
CHEST DISCOMFORT ( 353 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 352 FDA reports)
PAIN IN JAW ( 350 FDA reports)
DRUG TOXICITY ( 346 FDA reports)
BONE DISORDER ( 340 FDA reports)
PULMONARY OEDEMA ( 340 FDA reports)
BLOOD PRESSURE INCREASED ( 336 FDA reports)
OVERDOSE ( 332 FDA reports)
DIABETES MELLITUS ( 330 FDA reports)
CARDIAC DISORDER ( 326 FDA reports)
CARDIO-RESPIRATORY ARREST ( 325 FDA reports)
HEART RATE IRREGULAR ( 325 FDA reports)
BALANCE DISORDER ( 314 FDA reports)
SINUSITIS ( 313 FDA reports)
HYPERLIPIDAEMIA ( 308 FDA reports)
OSTEONECROSIS ( 308 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 307 FDA reports)
CEREBRAL INFARCTION ( 305 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 305 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 300 FDA reports)
HAEMATOCHEZIA ( 299 FDA reports)
HYPOKALAEMIA ( 299 FDA reports)
OSTEOMYELITIS ( 299 FDA reports)
JOINT SWELLING ( 298 FDA reports)
CARDIOMYOPATHY ( 297 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 297 FDA reports)
HYPOXIA ( 295 FDA reports)
SPINAL OSTEOARTHRITIS ( 295 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 294 FDA reports)
MULTIPLE INJURIES ( 294 FDA reports)
DYSPNOEA EXERTIONAL ( 293 FDA reports)
ASTHMA ( 292 FDA reports)
MULTI-ORGAN FAILURE ( 291 FDA reports)
HYPOGLYCAEMIA ( 290 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 289 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 287 FDA reports)
HAEMATEMESIS ( 285 FDA reports)
LETHARGY ( 283 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 282 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 282 FDA reports)
HALLUCINATION ( 281 FDA reports)
HYPERSENSITIVITY ( 280 FDA reports)
RHABDOMYOLYSIS ( 279 FDA reports)
SUBDURAL HAEMATOMA ( 278 FDA reports)
ABDOMINAL DISTENSION ( 277 FDA reports)
CHILLS ( 277 FDA reports)
CATARACT ( 273 FDA reports)
DISEASE PROGRESSION ( 272 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 271 FDA reports)
MUSCULOSKELETAL PAIN ( 271 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 269 FDA reports)
AMNESIA ( 266 FDA reports)
ANOREXIA ( 258 FDA reports)
STAPHYLOCOCCAL INFECTION ( 257 FDA reports)
MOBILITY DECREASED ( 256 FDA reports)
TOOTH EXTRACTION ( 254 FDA reports)
VISUAL IMPAIRMENT ( 254 FDA reports)
MEMORY IMPAIRMENT ( 253 FDA reports)
METASTASES TO BONE ( 247 FDA reports)
NEOPLASM MALIGNANT ( 247 FDA reports)
HYPOTHYROIDISM ( 245 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 245 FDA reports)
ABASIA ( 242 FDA reports)
DYSARTHRIA ( 242 FDA reports)
LIVER DISORDER ( 239 FDA reports)
CHOLELITHIASIS ( 235 FDA reports)
NECK PAIN ( 234 FDA reports)
ARTERIOSCLEROSIS ( 232 FDA reports)
DEFORMITY ( 232 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 231 FDA reports)
UNEVALUABLE EVENT ( 229 FDA reports)
TREATMENT NONCOMPLIANCE ( 227 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 227 FDA reports)
HEART RATE DECREASED ( 226 FDA reports)
CARDIAC MURMUR ( 223 FDA reports)
UNRESPONSIVE TO STIMULI ( 219 FDA reports)
VENTRICULAR FIBRILLATION ( 219 FDA reports)
IMPAIRED HEALING ( 218 FDA reports)
INCORRECT DOSE ADMINISTERED ( 216 FDA reports)
SKIN ULCER ( 216 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 215 FDA reports)
GASTRITIS ( 215 FDA reports)
BLOOD BILIRUBIN INCREASED ( 213 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 213 FDA reports)
ATRIAL FLUTTER ( 212 FDA reports)
HIATUS HERNIA ( 210 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 210 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 210 FDA reports)
ARTHRITIS ( 209 FDA reports)
EJECTION FRACTION DECREASED ( 208 FDA reports)
DIVERTICULUM ( 206 FDA reports)
RIB FRACTURE ( 204 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 203 FDA reports)
MEDICATION ERROR ( 203 FDA reports)
ABDOMINAL DISCOMFORT ( 202 FDA reports)
GINGIVAL BLEEDING ( 202 FDA reports)
AGITATION ( 201 FDA reports)
BONE PAIN ( 201 FDA reports)
FAECES DISCOLOURED ( 201 FDA reports)
HYPOPHAGIA ( 201 FDA reports)
SKIN DISCOLOURATION ( 200 FDA reports)
ALOPECIA ( 199 FDA reports)
ECCHYMOSIS ( 199 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 199 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 196 FDA reports)
HAEMORRHOIDS ( 196 FDA reports)
OSTEOPENIA ( 196 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 196 FDA reports)
SEPTIC SHOCK ( 193 FDA reports)
FLUID RETENTION ( 193 FDA reports)
MULTIPLE MYELOMA ( 193 FDA reports)
BLOOD POTASSIUM INCREASED ( 192 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 190 FDA reports)
DELIRIUM ( 190 FDA reports)
OSTEOPOROSIS ( 190 FDA reports)
URINARY RETENTION ( 190 FDA reports)
RENAL DISORDER ( 189 FDA reports)
SURGERY ( 188 FDA reports)
URTICARIA ( 188 FDA reports)
SHOCK ( 187 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 185 FDA reports)
DYSPEPSIA ( 185 FDA reports)
HERPES ZOSTER ( 185 FDA reports)
DRY MOUTH ( 184 FDA reports)
BLOOD POTASSIUM DECREASED ( 183 FDA reports)
BONE LESION ( 183 FDA reports)
DRUG EFFECT DECREASED ( 183 FDA reports)
DYSURIA ( 183 FDA reports)
LYMPHADENOPATHY ( 183 FDA reports)
WHEEZING ( 183 FDA reports)
ASCITES ( 182 FDA reports)
SLEEP APNOEA SYNDROME ( 181 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 180 FDA reports)
MUSCLE HAEMORRHAGE ( 178 FDA reports)
VISUAL ACUITY REDUCED ( 178 FDA reports)
HYPERGLYCAEMIA ( 177 FDA reports)
OXYGEN SATURATION DECREASED ( 177 FDA reports)
SWELLING FACE ( 176 FDA reports)
RETROPERITONEAL HAEMATOMA ( 174 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 174 FDA reports)
LEUKOPENIA ( 174 FDA reports)
PERICARDIAL EFFUSION ( 174 FDA reports)
DYSGEUSIA ( 173 FDA reports)
RENAL CYST ( 172 FDA reports)
BURNING SENSATION ( 170 FDA reports)
EXOSTOSIS ( 167 FDA reports)
VERTIGO ( 167 FDA reports)
GOUT ( 166 FDA reports)
COMA ( 165 FDA reports)
DENTAL CARIES ( 165 FDA reports)
DISABILITY ( 165 FDA reports)
BLOOD SODIUM DECREASED ( 164 FDA reports)
OFF LABEL USE ( 164 FDA reports)
FLUID OVERLOAD ( 163 FDA reports)
HEPATIC FAILURE ( 163 FDA reports)
HIP FRACTURE ( 163 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 163 FDA reports)
RESPIRATORY ARREST ( 163 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 162 FDA reports)
HEPATIC ENZYME INCREASED ( 162 FDA reports)
POST PROCEDURAL COMPLICATION ( 161 FDA reports)
HAEMODIALYSIS ( 160 FDA reports)
INFLAMMATION ( 160 FDA reports)
NASOPHARYNGITIS ( 160 FDA reports)
ANGINA PECTORIS ( 159 FDA reports)
METABOLIC ACIDOSIS ( 159 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 159 FDA reports)
SPEECH DISORDER ( 158 FDA reports)
DRUG HYPERSENSITIVITY ( 157 FDA reports)
HEAD INJURY ( 156 FDA reports)
FEBRILE NEUTROPENIA ( 154 FDA reports)
GASTRIC ULCER ( 154 FDA reports)
PRESYNCOPE ( 154 FDA reports)
SKIN NECROSIS ( 154 FDA reports)
RESPIRATORY DISTRESS ( 153 FDA reports)
COMPLETED SUICIDE ( 153 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 152 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 152 FDA reports)
PRODUCT QUALITY ISSUE ( 151 FDA reports)
URINARY INCONTINENCE ( 151 FDA reports)
PRIMARY SEQUESTRUM ( 149 FDA reports)
EXPOSED BONE IN JAW ( 149 FDA reports)
FEELING HOT ( 149 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 147 FDA reports)
CARDIOGENIC SHOCK ( 147 FDA reports)
JAUNDICE ( 145 FDA reports)
RIGHT VENTRICULAR FAILURE ( 145 FDA reports)
LEUKOCYTOSIS ( 144 FDA reports)
DISORIENTATION ( 143 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 143 FDA reports)
MYOCARDIAL ISCHAEMIA ( 143 FDA reports)
PNEUMONIA ASPIRATION ( 143 FDA reports)
BURSITIS ( 141 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 141 FDA reports)
OROPHARYNGEAL PAIN ( 141 FDA reports)
PATHOLOGICAL FRACTURE ( 141 FDA reports)
MALNUTRITION ( 140 FDA reports)
PANCREATITIS ( 140 FDA reports)
RASH PRURITIC ( 140 FDA reports)
DIVERTICULITIS ( 139 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 137 FDA reports)
PRODUCTIVE COUGH ( 137 FDA reports)
LUNG DISORDER ( 136 FDA reports)
SUDDEN DEATH ( 135 FDA reports)
SUICIDAL IDEATION ( 133 FDA reports)
RHINORRHOEA ( 132 FDA reports)
FLATULENCE ( 132 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 132 FDA reports)
LUNG INFILTRATION ( 132 FDA reports)
NASAL CONGESTION ( 132 FDA reports)
IRON DEFICIENCY ANAEMIA ( 130 FDA reports)
BLOOD GLUCOSE DECREASED ( 129 FDA reports)
DECREASED INTEREST ( 129 FDA reports)
SKIN INDURATION ( 129 FDA reports)
DYSSTASIA ( 128 FDA reports)
CIRCULATORY COLLAPSE ( 127 FDA reports)
EMPHYSEMA ( 127 FDA reports)
ILL-DEFINED DISORDER ( 127 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 127 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 126 FDA reports)
APHASIA ( 126 FDA reports)
DISCOMFORT ( 125 FDA reports)
ENCEPHALOPATHY ( 125 FDA reports)
PALLOR ( 125 FDA reports)
COLONIC POLYP ( 124 FDA reports)
STRESS ( 124 FDA reports)
DRUG LEVEL INCREASED ( 123 FDA reports)
HEPATITIS ( 123 FDA reports)
COMPRESSION FRACTURE ( 122 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 122 FDA reports)
INTESTINAL OBSTRUCTION ( 122 FDA reports)
PULMONARY CONGESTION ( 122 FDA reports)
RASH GENERALISED ( 122 FDA reports)
TYPE 2 DIABETES MELLITUS ( 122 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 121 FDA reports)
TOOTHACHE ( 121 FDA reports)
NEPHROLITHIASIS ( 121 FDA reports)
BLISTER ( 120 FDA reports)
LOOSE TOOTH ( 120 FDA reports)
SKIN EXFOLIATION ( 120 FDA reports)
RHEUMATOID ARTHRITIS ( 119 FDA reports)
TORSADE DE POINTES ( 119 FDA reports)
BLOOD URINE PRESENT ( 118 FDA reports)
DYSPHONIA ( 118 FDA reports)
HYPERCHOLESTEROLAEMIA ( 118 FDA reports)
ERECTILE DYSFUNCTION ( 116 FDA reports)
PHYSICAL DISABILITY ( 116 FDA reports)
SCOLIOSIS ( 116 FDA reports)
SPINAL COMPRESSION FRACTURE ( 115 FDA reports)
COAGULATION TIME PROLONGED ( 115 FDA reports)
BLINDNESS ( 114 FDA reports)
BLOOD ALBUMIN DECREASED ( 114 FDA reports)
PNEUMONITIS ( 114 FDA reports)
POLLAKIURIA ( 114 FDA reports)
TINNITUS ( 113 FDA reports)
ORTHOSTATIC HYPOTENSION ( 113 FDA reports)
OSTEOLYSIS ( 113 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 112 FDA reports)
PULMONARY FIBROSIS ( 112 FDA reports)
STOMATITIS ( 112 FDA reports)
AORTIC VALVE INCOMPETENCE ( 111 FDA reports)
FEAR ( 111 FDA reports)
GANGRENE ( 111 FDA reports)
MENTAL DISORDER ( 110 FDA reports)
HOT FLUSH ( 108 FDA reports)
INJECTION SITE PAIN ( 108 FDA reports)
SINUS BRADYCARDIA ( 108 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 106 FDA reports)
TOOTH DISORDER ( 106 FDA reports)
ABNORMAL BEHAVIOUR ( 106 FDA reports)
ACUTE RESPIRATORY FAILURE ( 106 FDA reports)
AZOTAEMIA ( 106 FDA reports)
BLOOD CALCIUM DECREASED ( 106 FDA reports)
COLD SWEAT ( 106 FDA reports)
DRY SKIN ( 106 FDA reports)
GENERALISED OEDEMA ( 106 FDA reports)
DIPLOPIA ( 105 FDA reports)
HEMIPARESIS ( 105 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 105 FDA reports)
NEUTROPHIL COUNT DECREASED ( 105 FDA reports)
TOOTH LOSS ( 105 FDA reports)
SINUS TACHYCARDIA ( 104 FDA reports)
ARTHROPATHY ( 104 FDA reports)
DEAFNESS ( 104 FDA reports)
GASTROINTESTINAL DISORDER ( 104 FDA reports)
HEPATIC STEATOSIS ( 104 FDA reports)
INFLUENZA ( 104 FDA reports)
LUNG NEOPLASM ( 104 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 103 FDA reports)
ROTATOR CUFF SYNDROME ( 103 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 102 FDA reports)
COGNITIVE DISORDER ( 102 FDA reports)
CORONARY ARTERY OCCLUSION ( 102 FDA reports)
DECUBITUS ULCER ( 102 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 102 FDA reports)
OBESITY ( 102 FDA reports)
COLITIS ( 101 FDA reports)
EAR PAIN ( 101 FDA reports)
HYPERTHYROIDISM ( 101 FDA reports)
ISCHAEMIC STROKE ( 101 FDA reports)
PULMONARY HAEMORRHAGE ( 101 FDA reports)
SKIN LESION ( 101 FDA reports)
TOOTH ABSCESS ( 101 FDA reports)
SICK SINUS SYNDROME ( 100 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 100 FDA reports)
DEMENTIA ( 100 FDA reports)
FEELING COLD ( 100 FDA reports)
MYELODYSPLASTIC SYNDROME ( 100 FDA reports)
OESOPHAGITIS ( 100 FDA reports)
LACERATION ( 99 FDA reports)
PURPURA ( 99 FDA reports)
PROSTATE CANCER ( 98 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 98 FDA reports)
MIGRAINE ( 98 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 97 FDA reports)
DISTURBANCE IN ATTENTION ( 97 FDA reports)
HYPOCALCAEMIA ( 97 FDA reports)
IRRITABILITY ( 97 FDA reports)
NERVOUSNESS ( 97 FDA reports)
NEURALGIA ( 97 FDA reports)
SCAR ( 97 FDA reports)
SLEEP DISORDER ( 97 FDA reports)
TENDERNESS ( 96 FDA reports)
DYSKINESIA ( 96 FDA reports)
CARPAL TUNNEL SYNDROME ( 95 FDA reports)
PNEUMOTHORAX ( 95 FDA reports)
CARDIAC VALVE DISEASE ( 94 FDA reports)
INJECTION SITE HAEMORRHAGE ( 93 FDA reports)
CANDIDIASIS ( 92 FDA reports)
DRUG DOSE OMISSION ( 92 FDA reports)
PULSE ABSENT ( 92 FDA reports)
ROAD TRAFFIC ACCIDENT ( 92 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 92 FDA reports)
EMBOLISM ( 91 FDA reports)
MASTICATION DISORDER ( 91 FDA reports)
AORTIC ANEURYSM ( 90 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 90 FDA reports)
EATING DISORDER ( 90 FDA reports)
ABSCESS ( 89 FDA reports)
FEMUR FRACTURE ( 89 FDA reports)
HAEMORRHAGIC DIATHESIS ( 89 FDA reports)
INFLUENZA LIKE ILLNESS ( 89 FDA reports)
JOINT STIFFNESS ( 89 FDA reports)
MASS ( 89 FDA reports)
RASH ERYTHEMATOUS ( 89 FDA reports)
CHOLECYSTITIS ( 88 FDA reports)
CYANOSIS ( 88 FDA reports)
DIALYSIS ( 88 FDA reports)
DRY EYE ( 88 FDA reports)
FISTULA ( 88 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 88 FDA reports)
NO THERAPEUTIC RESPONSE ( 88 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 87 FDA reports)
HYPOVOLAEMIA ( 87 FDA reports)
LOBAR PNEUMONIA ( 87 FDA reports)
MOVEMENT DISORDER ( 87 FDA reports)
ORAL INTAKE REDUCED ( 87 FDA reports)
ANURIA ( 86 FDA reports)
ATRIOVENTRICULAR BLOCK ( 86 FDA reports)
BODY TEMPERATURE INCREASED ( 86 FDA reports)
BONE MARROW FAILURE ( 86 FDA reports)
CARDIAC PACEMAKER INSERTION ( 86 FDA reports)
HYPOVOLAEMIC SHOCK ( 86 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 85 FDA reports)
ADVERSE EVENT ( 85 FDA reports)
BASAL CELL CARCINOMA ( 85 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 85 FDA reports)
DISEASE RECURRENCE ( 85 FDA reports)
GASTRITIS EROSIVE ( 85 FDA reports)
MOUTH HAEMORRHAGE ( 85 FDA reports)
PETECHIAE ( 85 FDA reports)
RESTLESSNESS ( 85 FDA reports)
SKIN DISORDER ( 85 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 84 FDA reports)
HAEMORRHAGIC STROKE ( 84 FDA reports)
METASTASES TO LIVER ( 84 FDA reports)
MUCOSAL INFLAMMATION ( 84 FDA reports)
ORTHOPNOEA ( 84 FDA reports)
ACCIDENTAL OVERDOSE ( 83 FDA reports)
GALLBLADDER DISORDER ( 83 FDA reports)
METASTASES TO SPINE ( 83 FDA reports)
MYOPATHY ( 83 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 83 FDA reports)
PHARYNGEAL OEDEMA ( 83 FDA reports)
PROTEINURIA ( 83 FDA reports)
VENTRICULAR HYPERTROPHY ( 83 FDA reports)
PLATELET COUNT INCREASED ( 82 FDA reports)
VIRAL INFECTION ( 82 FDA reports)
OCCULT BLOOD POSITIVE ( 82 FDA reports)
ORAL CANDIDIASIS ( 82 FDA reports)
ORAL DISORDER ( 82 FDA reports)
SYNOVIAL CYST ( 81 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 80 FDA reports)
AGGRESSION ( 80 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 80 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 80 FDA reports)
GLAUCOMA ( 80 FDA reports)
ATAXIA ( 79 FDA reports)
DEPRESSED MOOD ( 79 FDA reports)
HYPOMAGNESAEMIA ( 79 FDA reports)
LABORATORY TEST ABNORMAL ( 79 FDA reports)
PERIPHERAL COLDNESS ( 79 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 79 FDA reports)
SUICIDE ATTEMPT ( 79 FDA reports)
URINE OUTPUT DECREASED ( 79 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 78 FDA reports)
ASPIRATION ( 78 FDA reports)
CAROTID ARTERY STENOSIS ( 78 FDA reports)
HYPERCALCAEMIA ( 78 FDA reports)
ABDOMINAL TENDERNESS ( 77 FDA reports)
CEREBRAL ATROPHY ( 77 FDA reports)
EYE HAEMORRHAGE ( 77 FDA reports)
HEPATITIS ACUTE ( 77 FDA reports)
LUNG NEOPLASM MALIGNANT ( 77 FDA reports)
ORAL PAIN ( 77 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 76 FDA reports)
CALCIPHYLAXIS ( 76 FDA reports)
DIASTOLIC DYSFUNCTION ( 76 FDA reports)
DILATATION ATRIAL ( 76 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 75 FDA reports)
EMOTIONAL DISORDER ( 75 FDA reports)
OLIGURIA ( 75 FDA reports)
SWOLLEN TONGUE ( 75 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 75 FDA reports)
VAGINAL HAEMORRHAGE ( 75 FDA reports)
SPONDYLOLISTHESIS ( 74 FDA reports)
CHROMATURIA ( 74 FDA reports)
DIVERTICULUM INTESTINAL ( 74 FDA reports)
LIFE EXPECTANCY SHORTENED ( 74 FDA reports)
NOCTURIA ( 74 FDA reports)
OSTEOSCLEROSIS ( 74 FDA reports)
CARDIOVASCULAR DISORDER ( 73 FDA reports)
CATARACT OPERATION ( 73 FDA reports)
COORDINATION ABNORMAL ( 73 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 73 FDA reports)
MUSCLE TWITCHING ( 73 FDA reports)
NEOPLASM PROGRESSION ( 73 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 73 FDA reports)
TOOTH INFECTION ( 73 FDA reports)
VISUAL DISTURBANCE ( 73 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 72 FDA reports)
SPINAL COLUMN STENOSIS ( 72 FDA reports)
STEVENS-JOHNSON SYNDROME ( 72 FDA reports)
BONE DENSITY DECREASED ( 72 FDA reports)
CYSTITIS ( 72 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 72 FDA reports)
EYE PAIN ( 72 FDA reports)
AGRANULOCYTOSIS ( 71 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 71 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 71 FDA reports)
HAEMOLYSIS ( 71 FDA reports)
MACULAR DEGENERATION ( 71 FDA reports)
ORAL CAVITY FISTULA ( 71 FDA reports)
PROTHROMBIN TIME SHORTENED ( 71 FDA reports)
RETINAL HAEMORRHAGE ( 71 FDA reports)
THIRST ( 70 FDA reports)
VASCULITIS ( 70 FDA reports)
GOITRE ( 70 FDA reports)
HAEMARTHROSIS ( 70 FDA reports)
HEPATIC CYST ( 70 FDA reports)
JAW DISORDER ( 70 FDA reports)
LACTIC ACIDOSIS ( 70 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 70 FDA reports)
PANCREATITIS ACUTE ( 70 FDA reports)
DRUG ADMINISTRATION ERROR ( 69 FDA reports)
DYSLIPIDAEMIA ( 69 FDA reports)
HAEMOTHORAX ( 69 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 69 FDA reports)
LIMB INJURY ( 69 FDA reports)
DILATATION VENTRICULAR ( 68 FDA reports)
GINGIVAL SWELLING ( 68 FDA reports)
ILEUS ( 68 FDA reports)
INTRACARDIAC THROMBUS ( 68 FDA reports)
SKIN CANCER ( 68 FDA reports)
SKIN HYPERTROPHY ( 68 FDA reports)
PSORIASIS ( 67 FDA reports)
CLOSTRIDIAL INFECTION ( 67 FDA reports)
COLON CANCER ( 67 FDA reports)
DEVICE RELATED INFECTION ( 67 FDA reports)
FIBROSIS ( 67 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 67 FDA reports)
LEFT ATRIAL DILATATION ( 67 FDA reports)
LUMBAR SPINAL STENOSIS ( 67 FDA reports)
METASTASES TO LUNG ( 67 FDA reports)
NIGHT SWEATS ( 67 FDA reports)
OCULAR HYPERAEMIA ( 67 FDA reports)
BREAST CANCER ( 66 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 66 FDA reports)
GINGIVITIS ( 66 FDA reports)
KYPHOSIS ( 66 FDA reports)
LYMPHOEDEMA ( 66 FDA reports)
NEUTROPENIC SEPSIS ( 66 FDA reports)
PRURITUS GENERALISED ( 66 FDA reports)
SUBDURAL HAEMORRHAGE ( 65 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 65 FDA reports)
DRUG DISPENSING ERROR ( 65 FDA reports)
FIBROMYALGIA ( 65 FDA reports)
NERVOUS SYSTEM DISORDER ( 65 FDA reports)
CARDIAC FAILURE CHRONIC ( 64 FDA reports)
CEREBRAL ISCHAEMIA ( 64 FDA reports)
DEBRIDEMENT ( 64 FDA reports)
GRAND MAL CONVULSION ( 64 FDA reports)
PULMONARY THROMBOSIS ( 64 FDA reports)
RALES ( 64 FDA reports)
RENAL TUBULAR NECROSIS ( 64 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 64 FDA reports)
VENTRICULAR HYPOKINESIA ( 64 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 63 FDA reports)
RESPIRATORY DISORDER ( 63 FDA reports)
UPPER LIMB FRACTURE ( 63 FDA reports)
WOUND ( 63 FDA reports)
ANGINA UNSTABLE ( 63 FDA reports)
BACTERIAL INFECTION ( 62 FDA reports)
BLOOD DISORDER ( 62 FDA reports)
BONE DEBRIDEMENT ( 62 FDA reports)
DEAFNESS NEUROSENSORY ( 62 FDA reports)
GASTROENTERITIS ( 62 FDA reports)
INFUSION RELATED REACTION ( 62 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 62 FDA reports)
TOOTH FRACTURE ( 62 FDA reports)
ULCER ( 62 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 61 FDA reports)
RASH MACULO-PAPULAR ( 61 FDA reports)
SCIATICA ( 61 FDA reports)
SINUS DISORDER ( 61 FDA reports)
SQUAMOUS CELL CARCINOMA ( 61 FDA reports)
TRANSAMINASES INCREASED ( 61 FDA reports)
ABDOMINAL PAIN LOWER ( 61 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 61 FDA reports)
GROIN PAIN ( 61 FDA reports)
MOUTH ULCERATION ( 61 FDA reports)
AORTIC STENOSIS ( 60 FDA reports)
BACTERAEMIA ( 60 FDA reports)
DUODENAL ULCER ( 60 FDA reports)
ECZEMA ( 60 FDA reports)
HYPOKINESIA ( 60 FDA reports)
MENTAL IMPAIRMENT ( 60 FDA reports)
RESPIRATORY RATE INCREASED ( 60 FDA reports)
VISUAL FIELD DEFECT ( 60 FDA reports)
PERIODONTITIS ( 59 FDA reports)
PHARYNGITIS ( 59 FDA reports)
SKIN FIBROSIS ( 59 FDA reports)
WALKING AID USER ( 59 FDA reports)
ANEURYSM ( 59 FDA reports)
BRAIN OEDEMA ( 59 FDA reports)
DRUG RESISTANCE ( 59 FDA reports)
PERIODONTAL DISEASE ( 59 FDA reports)
HEPATIC CONGESTION ( 58 FDA reports)
INJECTION SITE ERYTHEMA ( 58 FDA reports)
LARYNGITIS ( 58 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 58 FDA reports)
SKIN TIGHTNESS ( 58 FDA reports)
TACHYPNOEA ( 58 FDA reports)
RESTLESS LEGS SYNDROME ( 57 FDA reports)
RETCHING ( 57 FDA reports)
ABNORMAL DREAMS ( 57 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 57 FDA reports)
DRUG ERUPTION ( 57 FDA reports)
GINGIVAL ULCERATION ( 57 FDA reports)
GYNAECOMASTIA ( 57 FDA reports)
HYPOACUSIS ( 57 FDA reports)
ANGIOEDEMA ( 56 FDA reports)
EOSINOPHIL COUNT INCREASED ( 56 FDA reports)
FAMILY STRESS ( 56 FDA reports)
HYPERURICAEMIA ( 56 FDA reports)
IRRITABLE BOWEL SYNDROME ( 56 FDA reports)
LYMPHOMA ( 56 FDA reports)
OSTEITIS ( 56 FDA reports)
RASH MACULAR ( 56 FDA reports)
RENAL INJURY ( 56 FDA reports)
SPLENOMEGALY ( 56 FDA reports)
ACTINOMYCOSIS ( 55 FDA reports)
ADVERSE DRUG REACTION ( 55 FDA reports)
COMPARTMENT SYNDROME ( 55 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 55 FDA reports)
ENDODONTIC PROCEDURE ( 55 FDA reports)
HAEMORRHAGIC ANAEMIA ( 55 FDA reports)
INCREASED TENDENCY TO BRUISE ( 55 FDA reports)
JOINT CONTRACTURE ( 55 FDA reports)
BLINDNESS UNILATERAL ( 54 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 54 FDA reports)
ELECTROLYTE IMBALANCE ( 54 FDA reports)
FLANK PAIN ( 54 FDA reports)
FOOD INTERACTION ( 54 FDA reports)
GASTRIC DISORDER ( 54 FDA reports)
HYPOAESTHESIA ORAL ( 54 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 54 FDA reports)
INCONTINENCE ( 54 FDA reports)
JOINT EFFUSION ( 54 FDA reports)
JOINT INJURY ( 54 FDA reports)
LOCAL SWELLING ( 54 FDA reports)
OESOPHAGEAL ULCER ( 54 FDA reports)
PLEURITIC PAIN ( 54 FDA reports)
PREMATURE BABY ( 54 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 54 FDA reports)
QUALITY OF LIFE DECREASED ( 54 FDA reports)
RHINITIS ALLERGIC ( 54 FDA reports)
SPINAL CORD COMPRESSION ( 54 FDA reports)
SPINAL DISORDER ( 54 FDA reports)
THROAT IRRITATION ( 54 FDA reports)
SHOCK HAEMORRHAGIC ( 53 FDA reports)
SPINAL FRACTURE ( 53 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 53 FDA reports)
DERMATITIS ( 53 FDA reports)
DIFFICULTY IN WALKING ( 53 FDA reports)
FAILURE TO THRIVE ( 53 FDA reports)
INTENTIONAL DRUG MISUSE ( 53 FDA reports)
JAW OPERATION ( 53 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 53 FDA reports)
MITRAL VALVE DISEASE ( 53 FDA reports)
BRUXISM ( 52 FDA reports)
CARDIAC TAMPONADE ( 52 FDA reports)
CHEST X-RAY ABNORMAL ( 52 FDA reports)
FRACTURE ( 52 FDA reports)
HYPERCOAGULATION ( 52 FDA reports)
LOCALISED INFECTION ( 52 FDA reports)
PROCEDURAL COMPLICATION ( 52 FDA reports)
SINUS CONGESTION ( 52 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 51 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 51 FDA reports)
EXTRADURAL HAEMATOMA ( 51 FDA reports)
FACE OEDEMA ( 51 FDA reports)
INTESTINAL ISCHAEMIA ( 51 FDA reports)
ISCHAEMIA ( 51 FDA reports)
PERICARDIAL HAEMORRHAGE ( 51 FDA reports)
CARDIAC FAILURE ACUTE ( 50 FDA reports)
CHOLECYSTITIS ACUTE ( 50 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 50 FDA reports)
FAECAL INCONTINENCE ( 50 FDA reports)
GINGIVAL PAIN ( 50 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 50 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 50 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 50 FDA reports)
MEDICATION RESIDUE ( 50 FDA reports)
METABOLIC ENCEPHALOPATHY ( 50 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 50 FDA reports)
SKIN BURNING SENSATION ( 50 FDA reports)
SKIN LACERATION ( 50 FDA reports)
THYROID DISORDER ( 50 FDA reports)
PHLEBITIS ( 49 FDA reports)
PLASMACYTOMA ( 49 FDA reports)
POLYURIA ( 49 FDA reports)
RADIOTHERAPY ( 49 FDA reports)
ACUTE PULMONARY OEDEMA ( 49 FDA reports)
EXCORIATION ( 49 FDA reports)
HEPATOTOXICITY ( 49 FDA reports)
HOSPITALISATION ( 49 FDA reports)
HYPERSOMNIA ( 49 FDA reports)
INJECTION SITE HAEMATOMA ( 49 FDA reports)
INTERMITTENT CLAUDICATION ( 49 FDA reports)
KNEE ARTHROPLASTY ( 49 FDA reports)
BRONCHOPNEUMONIA ( 48 FDA reports)
CERVICAL SPINAL STENOSIS ( 48 FDA reports)
EXERCISE TOLERANCE DECREASED ( 48 FDA reports)
HALLUCINATION, VISUAL ( 48 FDA reports)
HEPATIC LESION ( 48 FDA reports)
HYPHAEMA ( 48 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 48 FDA reports)
INTENTIONAL OVERDOSE ( 48 FDA reports)
PARKINSON'S DISEASE ( 48 FDA reports)
PSYCHOTIC DISORDER ( 48 FDA reports)
SOCIAL PROBLEM ( 48 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 47 FDA reports)
PYELONEPHRITIS ( 47 FDA reports)
SEDATION ( 47 FDA reports)
VASCULAR CALCIFICATION ( 47 FDA reports)
ANAPHYLACTIC SHOCK ( 47 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 47 FDA reports)
BRONCHIECTASIS ( 47 FDA reports)
DRUG INTOLERANCE ( 47 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 47 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 47 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 47 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 47 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 47 FDA reports)
MUSCLE TIGHTNESS ( 47 FDA reports)
PARALYSIS ( 47 FDA reports)
AORTIC CALCIFICATION ( 46 FDA reports)
AORTIC DISSECTION ( 46 FDA reports)
CHRONIC SINUSITIS ( 46 FDA reports)
CYST ( 46 FDA reports)
HYPERPLASIA ( 46 FDA reports)
MUSCLE ATROPHY ( 46 FDA reports)
PURULENT DISCHARGE ( 46 FDA reports)
RHONCHI ( 46 FDA reports)
THROMBOSIS IN DEVICE ( 46 FDA reports)
TRISMUS ( 46 FDA reports)
PULMONARY MASS ( 45 FDA reports)
SKIN HAEMORRHAGE ( 45 FDA reports)
STOMACH DISCOMFORT ( 45 FDA reports)
THERAPY NON-RESPONDER ( 45 FDA reports)
BLOOD CHLORIDE DECREASED ( 45 FDA reports)
BODY HEIGHT DECREASED ( 45 FDA reports)
DENTAL OPERATION ( 45 FDA reports)
EXTRASYSTOLES ( 45 FDA reports)
GINGIVAL DISORDER ( 45 FDA reports)
JAW FRACTURE ( 45 FDA reports)
JUGULAR VEIN THROMBOSIS ( 45 FDA reports)
MITRAL VALVE CALCIFICATION ( 45 FDA reports)
ACTINIC KERATOSIS ( 44 FDA reports)
ANOXIC ENCEPHALOPATHY ( 44 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 44 FDA reports)
ENDOTRACHEAL INTUBATION ( 44 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 44 FDA reports)
EYE DISORDER ( 44 FDA reports)
HYDRONEPHROSIS ( 44 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 44 FDA reports)
MYOCLONUS ( 44 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 44 FDA reports)
POLYNEUROPATHY ( 44 FDA reports)
RESUSCITATION ( 44 FDA reports)
SENSORY LOSS ( 44 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 44 FDA reports)
THROMBOPHLEBITIS ( 44 FDA reports)
VENTRICULAR DYSFUNCTION ( 44 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 44 FDA reports)
PERITONITIS ( 43 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 43 FDA reports)
ADRENAL INSUFFICIENCY ( 43 FDA reports)
ANGER ( 43 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 43 FDA reports)
CARDIOVERSION ( 43 FDA reports)
DELUSION ( 43 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 43 FDA reports)
ENDOCARDITIS ( 43 FDA reports)
FACIAL BONES FRACTURE ( 43 FDA reports)
FUNGAL INFECTION ( 43 FDA reports)
HERNIA ( 43 FDA reports)
LOWER LIMB FRACTURE ( 43 FDA reports)
MIDDLE INSOMNIA ( 43 FDA reports)
MITRAL VALVE PROLAPSE ( 43 FDA reports)
ORAL SURGERY ( 43 FDA reports)
ORGAN FAILURE ( 43 FDA reports)
ABSCESS JAW ( 42 FDA reports)
ANAPHYLACTIC REACTION ( 42 FDA reports)
CHOLESTASIS ( 42 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 42 FDA reports)
ESCHERICHIA INFECTION ( 42 FDA reports)
GLOSSODYNIA ( 42 FDA reports)
HYPOPHOSPHATAEMIA ( 42 FDA reports)
INGUINAL HERNIA ( 42 FDA reports)
LEFT VENTRICULAR FAILURE ( 42 FDA reports)
MENORRHAGIA ( 42 FDA reports)
NEURITIS ( 42 FDA reports)
NEUTROPHIL COUNT INCREASED ( 42 FDA reports)
PROTEIN TOTAL DECREASED ( 42 FDA reports)
THYROID NEOPLASM ( 42 FDA reports)
UROSEPSIS ( 42 FDA reports)
VENOUS THROMBOSIS ( 42 FDA reports)
PERITONEAL HAEMORRHAGE ( 41 FDA reports)
SENSORY DISTURBANCE ( 41 FDA reports)
SKIN HYPERPIGMENTATION ( 41 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 41 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 41 FDA reports)
WOUND INFECTION ( 41 FDA reports)
APLASIA PURE RED CELL ( 41 FDA reports)
BEDRIDDEN ( 41 FDA reports)
BONE SCAN ABNORMAL ( 41 FDA reports)
DIZZINESS POSTURAL ( 41 FDA reports)
EOSINOPHILIA ( 41 FDA reports)
GASTRIC POLYPS ( 41 FDA reports)
HEPATIC CIRRHOSIS ( 41 FDA reports)
HEPATIC ENCEPHALOPATHY ( 41 FDA reports)
HEPATOMEGALY ( 41 FDA reports)
IMPAIRED DRIVING ABILITY ( 41 FDA reports)
LACRIMATION INCREASED ( 41 FDA reports)
LACUNAR INFARCTION ( 41 FDA reports)
LIVEDO RETICULARIS ( 41 FDA reports)
MALLORY-WEISS SYNDROME ( 41 FDA reports)
MYOSITIS ( 41 FDA reports)
NECROSIS ( 41 FDA reports)
NEPHROTIC SYNDROME ( 41 FDA reports)
ORAL INFECTION ( 41 FDA reports)
ACIDOSIS ( 40 FDA reports)
ACUTE CORONARY SYNDROME ( 40 FDA reports)
ANGIOPATHY ( 40 FDA reports)
BRAIN HERNIATION ( 40 FDA reports)
BREATH SOUNDS ABNORMAL ( 40 FDA reports)
CARDIAC OPERATION ( 40 FDA reports)
CARDIOACTIVE DRUG LEVEL DECREASED ( 40 FDA reports)
CATHETER RELATED COMPLICATION ( 40 FDA reports)
INTESTINAL PERFORATION ( 40 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 40 FDA reports)
LIP SWELLING ( 40 FDA reports)
OTITIS MEDIA ( 40 FDA reports)
PANIC ATTACK ( 40 FDA reports)
PERSONALITY CHANGE ( 40 FDA reports)
PNEUMONIA BACTERIAL ( 40 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 40 FDA reports)
RESPIRATORY TRACT INFECTION ( 40 FDA reports)
RHINITIS ( 40 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 40 FDA reports)
URETERIC OBSTRUCTION ( 40 FDA reports)
RENAL ATROPHY ( 39 FDA reports)
SINUS ARRHYTHMIA ( 39 FDA reports)
SKIN ATROPHY ( 39 FDA reports)
STEM CELL TRANSPLANT ( 39 FDA reports)
STREPTOCOCCAL INFECTION ( 39 FDA reports)
TENDONITIS ( 39 FDA reports)
TUMOUR HAEMORRHAGE ( 39 FDA reports)
VARICOSE VEIN ( 39 FDA reports)
ACNE ( 39 FDA reports)
AORTIC VALVE DISEASE ( 39 FDA reports)
ATROPHY ( 39 FDA reports)
BLOOD AMYLASE INCREASED ( 39 FDA reports)
CARDIAC OUTPUT DECREASED ( 39 FDA reports)
CROHN'S DISEASE ( 39 FDA reports)
CRYING ( 39 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 39 FDA reports)
HAEMODYNAMIC INSTABILITY ( 39 FDA reports)
HEPATITIS FULMINANT ( 39 FDA reports)
HYPOALBUMINAEMIA ( 39 FDA reports)
LIMB DISCOMFORT ( 39 FDA reports)
MALIGNANT MELANOMA ( 39 FDA reports)
MULTIPLE DRUG OVERDOSE ( 39 FDA reports)
MUSCLE DISORDER ( 39 FDA reports)
MUSCLE RIGIDITY ( 39 FDA reports)
NODULE ( 39 FDA reports)
PELVIC FRACTURE ( 39 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 38 FDA reports)
CYSTITIS INTERSTITIAL ( 38 FDA reports)
DECREASED ACTIVITY ( 38 FDA reports)
DIABETIC RETINOPATHY ( 38 FDA reports)
EYE SWELLING ( 38 FDA reports)
FIBRIN D DIMER INCREASED ( 38 FDA reports)
LUNG CONSOLIDATION ( 38 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 38 FDA reports)
PREGNANCY ( 38 FDA reports)
RESPIRATORY TRACT CONGESTION ( 38 FDA reports)
SCAB ( 38 FDA reports)
POTENTIATING DRUG INTERACTION ( 37 FDA reports)
PSEUDOMONAS INFECTION ( 37 FDA reports)
SEROTONIN SYNDROME ( 37 FDA reports)
VITREOUS FLOATERS ( 37 FDA reports)
ALVEOLOPLASTY ( 37 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 37 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 37 FDA reports)
CAROTID ARTERY DISEASE ( 37 FDA reports)
FOOT FRACTURE ( 37 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 37 FDA reports)
HEARING IMPAIRED ( 37 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 37 FDA reports)
BLOOD PRESSURE ABNORMAL ( 36 FDA reports)
BLUE TOE SYNDROME ( 36 FDA reports)
BONE SWELLING ( 36 FDA reports)
DENTURE WEARER ( 36 FDA reports)
DIABETIC NEUROPATHY ( 36 FDA reports)
EAR DISCOMFORT ( 36 FDA reports)
ENTEROCOCCAL INFECTION ( 36 FDA reports)
FRACTURED SACRUM ( 36 FDA reports)
GASTROENTERITIS VIRAL ( 36 FDA reports)
HAEMOLYTIC ANAEMIA ( 36 FDA reports)
HAEMORRHAGE URINARY TRACT ( 36 FDA reports)
HEMIPLEGIA ( 36 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 36 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 36 FDA reports)
IMPAIRED WORK ABILITY ( 36 FDA reports)
INITIAL INSOMNIA ( 36 FDA reports)
KIDNEY INFECTION ( 36 FDA reports)
MEDICAL DEVICE COMPLICATION ( 36 FDA reports)
MUSCLE STRAIN ( 36 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 36 FDA reports)
PROSTATOMEGALY ( 36 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 36 FDA reports)
VIITH NERVE PARALYSIS ( 36 FDA reports)
WOUND DEHISCENCE ( 36 FDA reports)
WOUND HAEMORRHAGE ( 36 FDA reports)
WRONG DRUG ADMINISTERED ( 36 FDA reports)
RADICULOPATHY ( 35 FDA reports)
RESPIRATORY DEPRESSION ( 35 FDA reports)
SUDDEN CARDIAC DEATH ( 35 FDA reports)
TARDIVE DYSKINESIA ( 35 FDA reports)
TENDON DISORDER ( 35 FDA reports)
TROPONIN INCREASED ( 35 FDA reports)
ALCOHOL USE ( 35 FDA reports)
APNOEA ( 35 FDA reports)
BLADDER CANCER ( 35 FDA reports)
BRAIN DEATH ( 35 FDA reports)
BRONCHOSPASM ( 35 FDA reports)
CATHETER RELATED INFECTION ( 35 FDA reports)
EPILEPSY ( 35 FDA reports)
GRANULOMA ( 35 FDA reports)
HIP ARTHROPLASTY ( 35 FDA reports)
HYDROCEPHALUS ( 35 FDA reports)
MENINGIOMA ( 35 FDA reports)
NIGHTMARE ( 35 FDA reports)
ORAL DISCOMFORT ( 35 FDA reports)
BLOOD CALCIUM INCREASED ( 34 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 34 FDA reports)
BLOOD URIC ACID INCREASED ( 34 FDA reports)
BREAST MASS ( 34 FDA reports)
COLITIS ISCHAEMIC ( 34 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 34 FDA reports)
DRUG PRESCRIBING ERROR ( 34 FDA reports)
EAR HAEMORRHAGE ( 34 FDA reports)
EYE IRRITATION ( 34 FDA reports)
HYPOVENTILATION ( 34 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 34 FDA reports)
LEG AMPUTATION ( 34 FDA reports)
OPEN WOUND ( 34 FDA reports)
PARANOIA ( 34 FDA reports)
PERIPHERAL ISCHAEMIA ( 34 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 34 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 34 FDA reports)
RASH PAPULAR ( 34 FDA reports)
VENTRICULAR ARRHYTHMIA ( 34 FDA reports)
PHOTOPHOBIA ( 33 FDA reports)
PLEURAL FIBROSIS ( 33 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 33 FDA reports)
SOFT TISSUE INFLAMMATION ( 33 FDA reports)
TONGUE ULCERATION ( 33 FDA reports)
TOXIC SKIN ERUPTION ( 33 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 33 FDA reports)
WRIST FRACTURE ( 33 FDA reports)
ATRIAL TACHYCARDIA ( 33 FDA reports)
BARRETT'S OESOPHAGUS ( 33 FDA reports)
BLOOD CREATINE INCREASED ( 33 FDA reports)
BLOOD MAGNESIUM DECREASED ( 33 FDA reports)
BONE NEOPLASM MALIGNANT ( 33 FDA reports)
BONE OPERATION ( 33 FDA reports)
BRADYARRHYTHMIA ( 33 FDA reports)
DIABETIC NEPHROPATHY ( 33 FDA reports)
HAEMATOMA INFECTION ( 33 FDA reports)
MYELOMA RECURRENCE ( 33 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 33 FDA reports)
NYSTAGMUS ( 33 FDA reports)
PAIN OF SKIN ( 33 FDA reports)
PEPTIC ULCER ( 33 FDA reports)
BACK DISORDER ( 32 FDA reports)
BLOOD TEST ABNORMAL ( 32 FDA reports)
CARDIOPULMONARY FAILURE ( 32 FDA reports)
CERVICOBRACHIAL SYNDROME ( 32 FDA reports)
CHOLECYSTECTOMY ( 32 FDA reports)
DEVICE MALFUNCTION ( 32 FDA reports)
GUILLAIN-BARRE SYNDROME ( 32 FDA reports)
HUNGER ( 32 FDA reports)
ISCHAEMIC HEPATITIS ( 32 FDA reports)
JOINT DISLOCATION ( 32 FDA reports)
MAJOR DEPRESSION ( 32 FDA reports)
MICTURITION URGENCY ( 32 FDA reports)
MOOD SWINGS ( 32 FDA reports)
NEOPLASM ( 32 FDA reports)
PYURIA ( 32 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 32 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 32 FDA reports)
PLEURISY ( 31 FDA reports)
PURULENCE ( 31 FDA reports)
VENOUS INSUFFICIENCY ( 31 FDA reports)
VITREOUS HAEMORRHAGE ( 31 FDA reports)
WOUND SECRETION ( 31 FDA reports)
BODY TEMPERATURE DECREASED ( 31 FDA reports)
CARDIAC FIBRILLATION ( 31 FDA reports)
COAGULATION TEST ABNORMAL ( 31 FDA reports)
COLON ADENOMA ( 31 FDA reports)
CORONARY ARTERY STENOSIS ( 31 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 31 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 31 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 31 FDA reports)
GASTRITIS HAEMORRHAGIC ( 31 FDA reports)
GASTROINTESTINAL NECROSIS ( 31 FDA reports)
HAND FRACTURE ( 31 FDA reports)
HYPERKERATOSIS ( 31 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 31 FDA reports)
ARTERIAL THROMBOSIS ( 30 FDA reports)
BRAIN INJURY ( 30 FDA reports)
BREATH ODOUR ( 30 FDA reports)
COLLAPSE OF LUNG ( 30 FDA reports)
CONDUCTION DISORDER ( 30 FDA reports)
ERUCTATION ( 30 FDA reports)
EYELID OEDEMA ( 30 FDA reports)
FACIAL PALSY ( 30 FDA reports)
FEMORAL NECK FRACTURE ( 30 FDA reports)
METASTATIC NEOPLASM ( 30 FDA reports)
MONOCLONAL IMMUNOGLOBULIN PRESENT ( 30 FDA reports)
NEUROPATHY ( 30 FDA reports)
OVARIAN CYST ( 30 FDA reports)
PERICARDITIS ( 30 FDA reports)
RENAL ARTERY STENOSIS ( 30 FDA reports)
PERIPHERAL EMBOLISM ( 29 FDA reports)
RECTAL POLYP ( 29 FDA reports)
RETINAL DETACHMENT ( 29 FDA reports)
ULCER HAEMORRHAGE ( 29 FDA reports)
WHEELCHAIR USER ( 29 FDA reports)
ACCIDENTAL EXPOSURE ( 29 FDA reports)
ANTICOAGULATION DRUG LEVEL BELOW THERAPEUTIC ( 29 FDA reports)
BLEPHARITIS ( 29 FDA reports)
BLOOD COUNT ABNORMAL ( 29 FDA reports)
BLOOD CULTURE POSITIVE ( 29 FDA reports)
BREAST CANCER FEMALE ( 29 FDA reports)
BRONCHITIS CHRONIC ( 29 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 29 FDA reports)
CATHETER SITE HAEMORRHAGE ( 29 FDA reports)
CHOKING ( 29 FDA reports)
DRUG INTERACTION POTENTIATION ( 29 FDA reports)
INCISIONAL DRAINAGE ( 29 FDA reports)
INFARCTION ( 29 FDA reports)
LIPASE INCREASED ( 29 FDA reports)
LUNG INFECTION ( 29 FDA reports)
MENINGITIS ( 29 FDA reports)
NEPHROPATHY ( 29 FDA reports)
NERVE INJURY ( 29 FDA reports)
OSTEORADIONECROSIS ( 29 FDA reports)
ABDOMINAL HERNIA ( 28 FDA reports)
ABORTION INDUCED ( 28 FDA reports)
ADNEXA UTERI MASS ( 28 FDA reports)
APATHY ( 28 FDA reports)
APHAGIA ( 28 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 28 FDA reports)
BONE NEOPLASM ( 28 FDA reports)
CORONARY ARTERY BYPASS ( 28 FDA reports)
DEAFNESS UNILATERAL ( 28 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 28 FDA reports)
DEVICE FAILURE ( 28 FDA reports)
DRUG DEPENDENCE ( 28 FDA reports)
DRUG LEVEL DECREASED ( 28 FDA reports)
DUODENITIS ( 28 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 28 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 28 FDA reports)
EMBOLISM VENOUS ( 28 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 28 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 28 FDA reports)
FLUID INTAKE REDUCED ( 28 FDA reports)
GINGIVAL RECESSION ( 28 FDA reports)
HYPERBILIRUBINAEMIA ( 28 FDA reports)
HYPERNATRAEMIA ( 28 FDA reports)
HYPERTHERMIA ( 28 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 28 FDA reports)
INCREASED APPETITE ( 28 FDA reports)
LIVER INJURY ( 28 FDA reports)
MENISCUS LESION ( 28 FDA reports)
NEPHRITIS INTERSTITIAL ( 28 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 28 FDA reports)
POOR QUALITY SLEEP ( 28 FDA reports)
PROTEIN URINE PRESENT ( 28 FDA reports)
RENAL CELL CARCINOMA ( 28 FDA reports)
RENAL HAEMORRHAGE ( 28 FDA reports)
STATUS EPILEPTICUS ( 28 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 28 FDA reports)
VERTEBROPLASTY ( 28 FDA reports)
RIGHT ATRIAL DILATATION ( 27 FDA reports)
SKIN PAPILLOMA ( 27 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 27 FDA reports)
SUPERIOR VENA CAVA SYNDROME ( 27 FDA reports)
TEMPERATURE INTOLERANCE ( 27 FDA reports)
VENA CAVA THROMBOSIS ( 27 FDA reports)
WEIGHT FLUCTUATION ( 27 FDA reports)
WITHDRAWAL SYNDROME ( 27 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 27 FDA reports)
ATRIAL THROMBOSIS ( 27 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 27 FDA reports)
BONE LOSS ( 27 FDA reports)
CEREBELLAR SYNDROME ( 27 FDA reports)
CHOLANGITIS ( 27 FDA reports)
CREPITATIONS ( 27 FDA reports)
DYSPHEMIA ( 27 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 27 FDA reports)
EMBOLIC STROKE ( 27 FDA reports)
ENTEROCOLITIS ( 27 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 27 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 27 FDA reports)
HYPOCOAGULABLE STATE ( 27 FDA reports)
HYPOTONIA ( 27 FDA reports)
IATROGENIC INJURY ( 27 FDA reports)
INCOHERENT ( 27 FDA reports)
INJECTION SITE PRURITUS ( 27 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 27 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 27 FDA reports)
MOTOR DYSFUNCTION ( 27 FDA reports)
NASAL SEPTUM DEVIATION ( 27 FDA reports)
PARAPARESIS ( 27 FDA reports)
PARONYCHIA ( 27 FDA reports)
ANKLE FRACTURE ( 26 FDA reports)
AORTIC DISORDER ( 26 FDA reports)
BREAST CANCER RECURRENT ( 26 FDA reports)
CACHEXIA ( 26 FDA reports)
CATHETER PLACEMENT ( 26 FDA reports)
CERUMEN IMPACTION ( 26 FDA reports)
COAGULATION TIME SHORTENED ( 26 FDA reports)
COR PULMONALE ( 26 FDA reports)
DERMATITIS EXFOLIATIVE ( 26 FDA reports)
EARLY SATIETY ( 26 FDA reports)
EPIGASTRIC DISCOMFORT ( 26 FDA reports)
EXTREMITY CONTRACTURE ( 26 FDA reports)
FOLLICULITIS ( 26 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 26 FDA reports)
GASTROINTESTINAL PERFORATION ( 26 FDA reports)
GRANULOCYTOPENIA ( 26 FDA reports)
HEART RATE ABNORMAL ( 26 FDA reports)
HYPERVENTILATION ( 26 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 26 FDA reports)
INTRAOCULAR LENS IMPLANT ( 26 FDA reports)
LARGE INTESTINAL ULCER ( 26 FDA reports)
LUNG CANCER METASTATIC ( 26 FDA reports)
MITRAL VALVE STENOSIS ( 26 FDA reports)
MYDRIASIS ( 26 FDA reports)
NEPHROSCLEROSIS ( 26 FDA reports)
NON-CARDIAC CHEST PAIN ( 26 FDA reports)
OCULAR ICTERUS ( 26 FDA reports)
OPEN REDUCTION OF FRACTURE ( 26 FDA reports)
POOR PERIPHERAL CIRCULATION ( 26 FDA reports)
PORTAL VEIN THROMBOSIS ( 26 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 26 FDA reports)
SENSITIVITY OF TEETH ( 26 FDA reports)
SEQUESTRECTOMY ( 26 FDA reports)
SUBCUTANEOUS ABSCESS ( 26 FDA reports)
TOOTH IMPACTED ( 26 FDA reports)
TUBERCULOSIS ( 26 FDA reports)
POLYP ( 25 FDA reports)
PULMONARY ARTERIAL PRESSURE INCREASED ( 25 FDA reports)
QUADRIPLEGIA ( 25 FDA reports)
SENSATION OF HEAVINESS ( 25 FDA reports)
SERRATIA BACTERAEMIA ( 25 FDA reports)
SMALL FOR DATES BABY ( 25 FDA reports)
SPINAL FUSION SURGERY ( 25 FDA reports)
SPUTUM DISCOLOURED ( 25 FDA reports)
TONGUE DISCOLOURATION ( 25 FDA reports)
VENOUS THROMBOSIS LIMB ( 25 FDA reports)
ACUTE PRERENAL FAILURE ( 25 FDA reports)
AORTIC VALVE SCLEROSIS ( 25 FDA reports)
CARDIOACTIVE DRUG LEVEL BELOW THERAPEUTIC ( 25 FDA reports)
CAROTID BRUIT ( 25 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 25 FDA reports)
CEREBROVASCULAR DISORDER ( 25 FDA reports)
DISSOCIATION ( 25 FDA reports)
EDENTULOUS ( 25 FDA reports)
EXFOLIATIVE RASH ( 25 FDA reports)
FACE INJURY ( 25 FDA reports)
HELICOBACTER INFECTION ( 25 FDA reports)
IMMUNODEFICIENCY ( 25 FDA reports)
METASTASIS ( 25 FDA reports)
NERVE COMPRESSION ( 25 FDA reports)
ABDOMINAL HAEMATOMA ( 24 FDA reports)
ABSCESS LIMB ( 24 FDA reports)
AGEUSIA ( 24 FDA reports)
CAESAREAN SECTION ( 24 FDA reports)
CARDIAC FLUTTER ( 24 FDA reports)
CEREBELLAR HAEMORRHAGE ( 24 FDA reports)
GASTROINTESTINAL ARTERIOVENOUS MALFORMATION ( 24 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 24 FDA reports)
HEPATITIS C ( 24 FDA reports)
HERPES SIMPLEX ( 24 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 24 FDA reports)
INTESTINAL HAEMORRHAGE ( 24 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 24 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 24 FDA reports)
NEPHROPATHY TOXIC ( 24 FDA reports)
OEDEMA MOUTH ( 24 FDA reports)
ONYCHOMYCOSIS ( 24 FDA reports)
POISONING ( 24 FDA reports)
SINUS HEADACHE ( 24 FDA reports)
SKIN WARM ( 24 FDA reports)
STENT PLACEMENT ( 24 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 24 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 24 FDA reports)
VEIN DISORDER ( 24 FDA reports)
PHOTOPSIA ( 23 FDA reports)
PREMATURE LABOUR ( 23 FDA reports)
RESPIRATORY RATE DECREASED ( 23 FDA reports)
SNEEZING ( 23 FDA reports)
THROAT TIGHTNESS ( 23 FDA reports)
TOBACCO ABUSE ( 23 FDA reports)
ABDOMINAL INFECTION ( 23 FDA reports)
ADRENAL DISORDER ( 23 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 23 FDA reports)
ANAEMIA OF MALIGNANT DISEASE ( 23 FDA reports)
AREFLEXIA ( 23 FDA reports)
ARTHRITIS BACTERIAL ( 23 FDA reports)
BLADDER DISORDER ( 23 FDA reports)
CATARACT NUCLEAR ( 23 FDA reports)
CATHETERISATION CARDIAC ( 23 FDA reports)
CHOLECYSTITIS CHRONIC ( 23 FDA reports)
CHOROIDAL HAEMORRHAGE ( 23 FDA reports)
DEVICE OCCLUSION ( 23 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 23 FDA reports)
DYSAESTHESIA ( 23 FDA reports)
DYSPNOEA EXACERBATED ( 23 FDA reports)
ESSENTIAL HYPERTENSION ( 23 FDA reports)
EXTREMITY NECROSIS ( 23 FDA reports)
FURUNCLE ( 23 FDA reports)
GENERALISED ERYTHEMA ( 23 FDA reports)
HEART INJURY ( 23 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 23 FDA reports)
LEUKAEMIA ( 23 FDA reports)
MUSCLE INJURY ( 23 FDA reports)
OSTEITIS DEFORMANS ( 23 FDA reports)
OVERWEIGHT ( 23 FDA reports)
PANCREATIC CARCINOMA ( 23 FDA reports)
PANCREATIC CYST ( 23 FDA reports)
PAROTITIS ( 23 FDA reports)
PELVIC PAIN ( 23 FDA reports)
ABDOMINAL ABSCESS ( 22 FDA reports)
ACUTE HEPATIC FAILURE ( 22 FDA reports)
BLOOD BLISTER ( 22 FDA reports)
BREAST PAIN ( 22 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 22 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 22 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 22 FDA reports)
CONTRAST MEDIA REACTION ( 22 FDA reports)
DIABETIC KETOACIDOSIS ( 22 FDA reports)
DRUG EFFECT INCREASED ( 22 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 22 FDA reports)
FACIAL PAIN ( 22 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 22 FDA reports)
INJECTION SITE EXTRAVASATION ( 22 FDA reports)
INJECTION SITE SWELLING ( 22 FDA reports)
LARGE INTESTINE PERFORATION ( 22 FDA reports)
LISTLESS ( 22 FDA reports)
METABOLIC SYNDROME ( 22 FDA reports)
METASTASES TO LYMPH NODES ( 22 FDA reports)
OSTEOCHONDROSIS ( 22 FDA reports)
PARAESTHESIA ORAL ( 22 FDA reports)
PULMONARY INFARCTION ( 22 FDA reports)
TENDON RUPTURE ( 22 FDA reports)
TOOTH EROSION ( 22 FDA reports)
URINE FLOW DECREASED ( 22 FDA reports)
PHOTOSENSITIVITY REACTION ( 21 FDA reports)
PLANTAR FASCIITIS ( 21 FDA reports)
POLYDIPSIA ( 21 FDA reports)
QRS AXIS ABNORMAL ( 21 FDA reports)
RENAL CANCER ( 21 FDA reports)
ROSACEA ( 21 FDA reports)
STASIS DERMATITIS ( 21 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 21 FDA reports)
THROMBOCYTOSIS ( 21 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 21 FDA reports)
ACCIDENT ( 21 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 21 FDA reports)
BLOOD CHLORIDE INCREASED ( 21 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 21 FDA reports)
CALCINOSIS ( 21 FDA reports)
COLITIS ULCERATIVE ( 21 FDA reports)
COSTOCHONDRITIS ( 21 FDA reports)
DEPRESSIVE SYMPTOM ( 21 FDA reports)
EXPIRED DRUG ADMINISTERED ( 21 FDA reports)
EYE INFLAMMATION ( 21 FDA reports)
FAECALOMA ( 21 FDA reports)
GASTROINTESTINAL PAIN ( 21 FDA reports)
HEPATITIS B ( 21 FDA reports)
HUMERUS FRACTURE ( 21 FDA reports)
MUSCLE CONTRACTURE ( 21 FDA reports)
PANCREATITIS CHRONIC ( 21 FDA reports)
PARAPLEGIA ( 21 FDA reports)
PAROTID GLAND ENLARGEMENT ( 21 FDA reports)
ABNORMAL FAECES ( 20 FDA reports)
ABSCESS DRAINAGE ( 20 FDA reports)
AFFECTIVE DISORDER ( 20 FDA reports)
AORTIC THROMBOSIS ( 20 FDA reports)
APHONIA ( 20 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 20 FDA reports)
ATRIAL SEPTAL DEFECT ( 20 FDA reports)
BACK INJURY ( 20 FDA reports)
BONE MARROW TRANSPLANT ( 20 FDA reports)
BREAST CANCER METASTATIC ( 20 FDA reports)
CEREBRAL HAEMATOMA ( 20 FDA reports)
CERVICAL CORD COMPRESSION ( 20 FDA reports)
COAGULATION TIME ABNORMAL ( 20 FDA reports)
CULTURE URINE POSITIVE ( 20 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 20 FDA reports)
DERMATITIS BULLOUS ( 20 FDA reports)
EAR INFECTION ( 20 FDA reports)
ERYTHEMA MULTIFORME ( 20 FDA reports)
GASTRIC CANCER ( 20 FDA reports)
GINGIVAL INFECTION ( 20 FDA reports)
HAEMANGIOMA ( 20 FDA reports)
HEART VALVE INCOMPETENCE ( 20 FDA reports)
HEART VALVE REPLACEMENT ( 20 FDA reports)
HYPOTHERMIA ( 20 FDA reports)
HYSTERECTOMY ( 20 FDA reports)
ILEUS PARALYTIC ( 20 FDA reports)
JUGULAR VEIN DISTENSION ( 20 FDA reports)
KLEBSIELLA SEPSIS ( 20 FDA reports)
MANIA ( 20 FDA reports)
NODAL RHYTHM ( 20 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 20 FDA reports)
OPTIC ATROPHY ( 20 FDA reports)
ORAL DISCHARGE ( 20 FDA reports)
PAPILLOMA ( 20 FDA reports)
PUPIL FIXED ( 20 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 20 FDA reports)
RENAL TUBULAR DISORDER ( 20 FDA reports)
SMALL INTESTINE CARCINOMA ( 20 FDA reports)
SPONDYLOLYSIS ( 20 FDA reports)
THINKING ABNORMAL ( 20 FDA reports)
TREATMENT FAILURE ( 20 FDA reports)
TUMOUR LYSIS SYNDROME ( 20 FDA reports)
VAGINAL DISCHARGE ( 20 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 19 FDA reports)
POST PROCEDURAL HAEMATOMA ( 19 FDA reports)
POSTURE ABNORMAL ( 19 FDA reports)
PROSTATISM ( 19 FDA reports)
PULMONARY TOXICITY ( 19 FDA reports)
PYELONEPHRITIS ACUTE ( 19 FDA reports)
SEBORRHOEIC DERMATITIS ( 19 FDA reports)
SECRETION DISCHARGE ( 19 FDA reports)
SPINAL CORPECTOMY ( 19 FDA reports)
SPLENIC LESION ( 19 FDA reports)
SPUTUM CULTURE POSITIVE ( 19 FDA reports)
STRESS URINARY INCONTINENCE ( 19 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 19 FDA reports)
TELANGIECTASIA ( 19 FDA reports)
TIBIA FRACTURE ( 19 FDA reports)
TRANSFUSION ( 19 FDA reports)
VASCULAR PSEUDOANEURYSM ( 19 FDA reports)
WEGENER'S GRANULOMATOSIS ( 19 FDA reports)
X-RAY ABNORMAL ( 19 FDA reports)
ABDOMINAL MASS ( 19 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 19 FDA reports)
APHTHOUS STOMATITIS ( 19 FDA reports)
ARTERIOVENOUS MALFORMATION ( 19 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 19 FDA reports)
BLOODY DISCHARGE ( 19 FDA reports)
BONE MARROW DEPRESSION ( 19 FDA reports)
ERYSIPELAS ( 19 FDA reports)
ESCHERICHIA TEST POSITIVE ( 19 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 19 FDA reports)
FAT EMBOLISM ( 19 FDA reports)
FEELING JITTERY ( 19 FDA reports)
HEPATIC MASS ( 19 FDA reports)
HYPERAMMONAEMIA ( 19 FDA reports)
IMMOBILE ( 19 FDA reports)
INFECTED SKIN ULCER ( 19 FDA reports)
INJECTION SITE REACTION ( 19 FDA reports)
INTRACRANIAL ANEURYSM ( 19 FDA reports)
LYMPHADENITIS ( 19 FDA reports)
MASTOIDITIS ( 19 FDA reports)
MULTIPLE SCLEROSIS ( 19 FDA reports)
NO ADVERSE EVENT ( 19 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 19 FDA reports)
PEMPHIGOID ( 19 FDA reports)
AORTIC VALVE STENOSIS ( 18 FDA reports)
ASPHYXIA ( 18 FDA reports)
BLOOD SODIUM INCREASED ( 18 FDA reports)
BLOOD UREA DECREASED ( 18 FDA reports)
BUNDLE BRANCH BLOCK ( 18 FDA reports)
CALCULUS URINARY ( 18 FDA reports)
CARDIAC HYPERTROPHY ( 18 FDA reports)
CEREBRAL THROMBOSIS ( 18 FDA reports)
CLOSTRIDIUM COLITIS ( 18 FDA reports)
DENTAL CARE ( 18 FDA reports)
DERMATITIS CONTACT ( 18 FDA reports)
DROP ATTACKS ( 18 FDA reports)
ENTEROCUTANEOUS FISTULA ( 18 FDA reports)
FOOT DEFORMITY ( 18 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 18 FDA reports)
GRIP STRENGTH DECREASED ( 18 FDA reports)
HAIR GROWTH ABNORMAL ( 18 FDA reports)
HILAR LYMPHADENOPATHY ( 18 FDA reports)
HYPERREFLEXIA ( 18 FDA reports)
HYPERTENSIVE HEART DISEASE ( 18 FDA reports)
INADEQUATE ANALGESIA ( 18 FDA reports)
INCISION SITE COMPLICATION ( 18 FDA reports)
INJECTION SITE BRUISING ( 18 FDA reports)
KLEBSIELLA INFECTION ( 18 FDA reports)
MONOCLONAL GAMMOPATHY ( 18 FDA reports)
MUSCULOSKELETAL DISORDER ( 18 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 18 FDA reports)
NEUROLOGICAL SYMPTOM ( 18 FDA reports)
PARTNER STRESS ( 18 FDA reports)
PO2 DECREASED ( 18 FDA reports)
PSORIATIC ARTHROPATHY ( 18 FDA reports)
REFLUX OESOPHAGITIS ( 18 FDA reports)
SCLERODERMA ( 18 FDA reports)
SCRATCH ( 18 FDA reports)
SEASONAL ALLERGY ( 18 FDA reports)
SEBORRHOEIC KERATOSIS ( 18 FDA reports)
SELF-MEDICATION ( 18 FDA reports)
SKIN PLAQUE ( 18 FDA reports)
SPINAL LAMINECTOMY ( 18 FDA reports)
TROPONIN I INCREASED ( 18 FDA reports)
UBIQUINONE DECREASED ( 18 FDA reports)
URINE ABNORMALITY ( 18 FDA reports)
VITAMIN D DEFICIENCY ( 18 FDA reports)
PERONEAL NERVE PALSY ( 17 FDA reports)
PIGMENTATION DISORDER ( 17 FDA reports)
POLYMYALGIA RHEUMATICA ( 17 FDA reports)
POST PROCEDURAL FISTULA ( 17 FDA reports)
PROCEDURAL PAIN ( 17 FDA reports)
PROSTATITIS ( 17 FDA reports)
PULMONARY RADIATION INJURY ( 17 FDA reports)
RADIAL NERVE PALSY ( 17 FDA reports)
RENAL PAIN ( 17 FDA reports)
SOFT TISSUE MASS ( 17 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 17 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 17 FDA reports)
ACROCHORDON ( 17 FDA reports)
ADRENAL MASS ( 17 FDA reports)
AORTIC VALVE CALCIFICATION ( 17 FDA reports)
APICECTOMY ( 17 FDA reports)
BACTERIAL DISEASE CARRIER ( 17 FDA reports)
BIPOLAR DISORDER ( 17 FDA reports)
BLEEDING TIME PROLONGED ( 17 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 17 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 17 FDA reports)
CANCER PAIN ( 17 FDA reports)
CEREBELLAR ISCHAEMIA ( 17 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 17 FDA reports)
CHEILITIS ( 17 FDA reports)
CHONDROCALCINOSIS ( 17 FDA reports)
CONJUNCTIVITIS ( 17 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 17 FDA reports)
DROOLING ( 17 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 17 FDA reports)
EAR DISORDER ( 17 FDA reports)
FACIAL PARESIS ( 17 FDA reports)
GASTROINTESTINAL INFECTION ( 17 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 17 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 17 FDA reports)
HEARING AID USER ( 17 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 17 FDA reports)
HEPATORENAL SYNDROME ( 17 FDA reports)
HYPOAESTHESIA FACIAL ( 17 FDA reports)
HYPOGLYCAEMIC COMA ( 17 FDA reports)
HYPOREFLEXIA ( 17 FDA reports)
INCISION SITE HAEMORRHAGE ( 17 FDA reports)
KIDNEY SMALL ( 17 FDA reports)
LEUKOENCEPHALOPATHY ( 17 FDA reports)
LIP OEDEMA ( 17 FDA reports)
LOSS OF EMPLOYMENT ( 17 FDA reports)
LYMPHOPENIA ( 17 FDA reports)
MECHANICAL VENTILATION ( 17 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 17 FDA reports)
METASTASES TO ADRENALS ( 17 FDA reports)
METASTATIC PAIN ( 17 FDA reports)
MYOPIA ( 17 FDA reports)
NECK INJURY ( 17 FDA reports)
NECROTISING FASCIITIS ( 17 FDA reports)
NEURODERMATITIS ( 17 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 17 FDA reports)
OTITIS EXTERNA ( 17 FDA reports)
PAROSMIA ( 17 FDA reports)
PERIARTHRITIS ( 17 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 16 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 16 FDA reports)
APPLICATION SITE PRURITUS ( 16 FDA reports)
ASTIGMATISM ( 16 FDA reports)
BENIGN OVARIAN TUMOUR ( 16 FDA reports)
BILIARY TRACT DISORDER ( 16 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 16 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 16 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 16 FDA reports)
BLOOD PH DECREASED ( 16 FDA reports)
BLOOD URINE ( 16 FDA reports)
BRAIN STEM HAEMORRHAGE ( 16 FDA reports)
BREAST ENLARGEMENT ( 16 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 16 FDA reports)
CARDIAC ENZYMES INCREASED ( 16 FDA reports)
CARDIAC VALVE VEGETATION ( 16 FDA reports)
CATHETER SEPSIS ( 16 FDA reports)
CENTRAL LINE INFECTION ( 16 FDA reports)
CEREBRAL DISORDER ( 16 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 16 FDA reports)
CHOKING SENSATION ( 16 FDA reports)
COLONIC STENOSIS ( 16 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 16 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 16 FDA reports)
CUSHINGOID ( 16 FDA reports)
DERMATITIS ALLERGIC ( 16 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 16 FDA reports)
EMBOLISM ARTERIAL ( 16 FDA reports)
EROSIVE OESOPHAGITIS ( 16 FDA reports)
EYE OPERATION ( 16 FDA reports)
FUNGAEMIA ( 16 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 16 FDA reports)
GASTROINTESTINAL ULCER ( 16 FDA reports)
GLOSSITIS ( 16 FDA reports)
HEPATITIS CHOLESTATIC ( 16 FDA reports)
HYDROPNEUMOTHORAX ( 16 FDA reports)
HYPERCAPNIA ( 16 FDA reports)
HYPERPHOSPHATAEMIA ( 16 FDA reports)
INJECTION SITE IRRITATION ( 16 FDA reports)
JOINT SPRAIN ( 16 FDA reports)
LARYNGEAL OEDEMA ( 16 FDA reports)
LIPOMA ( 16 FDA reports)
LIVER TRANSPLANT ( 16 FDA reports)
LONG QT SYNDROME ( 16 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 16 FDA reports)
MACULOPATHY ( 16 FDA reports)
METABOLIC DISORDER ( 16 FDA reports)
MONOPLEGIA ( 16 FDA reports)
NASAL DISORDER ( 16 FDA reports)
NEUROTOXICITY ( 16 FDA reports)
ODYNOPHAGIA ( 16 FDA reports)
OESOPHAGITIS ULCERATIVE ( 16 FDA reports)
PAPILLOEDEMA ( 16 FDA reports)
PELVIC HAEMATOMA ( 16 FDA reports)
PNEUMONIA KLEBSIELLA ( 16 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 16 FDA reports)
POOR DENTAL CONDITION ( 16 FDA reports)
POST HERPETIC NEURALGIA ( 16 FDA reports)
PRESBYOPIA ( 16 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 16 FDA reports)
RECTAL ULCER ( 16 FDA reports)
RESPIRATORY ACIDOSIS ( 16 FDA reports)
SERUM FERRITIN INCREASED ( 16 FDA reports)
SKIN IRRITATION ( 16 FDA reports)
SPINAL DECOMPRESSION ( 16 FDA reports)
SPINAL HAEMATOMA ( 16 FDA reports)
SPLENIC INFARCTION ( 16 FDA reports)
SYNOVIAL RUPTURE ( 16 FDA reports)
SYNOVITIS ( 16 FDA reports)
TETANY ( 16 FDA reports)
THYROIDITIS CHRONIC ( 16 FDA reports)
TONGUE DISORDER ( 16 FDA reports)
URINARY TRACT DISORDER ( 16 FDA reports)
URINE ANALYSIS ABNORMAL ( 16 FDA reports)
VENOUS OCCLUSION ( 16 FDA reports)
VITAMIN K DEFICIENCY ( 16 FDA reports)
PITTING OEDEMA ( 15 FDA reports)
POST THROMBOTIC SYNDROME ( 15 FDA reports)
PROTEIN URINE ( 15 FDA reports)
RED BLOOD CELL ABNORMALITY ( 15 FDA reports)
SINUS ARREST ( 15 FDA reports)
SKIN GRAFT ( 15 FDA reports)
SPINAL COLUMN INJURY ( 15 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 15 FDA reports)
TEMPORAL ARTERITIS ( 15 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 15 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 15 FDA reports)
TIC ( 15 FDA reports)
UNDERDOSE ( 15 FDA reports)
ABDOMINAL ADHESIONS ( 15 FDA reports)
ABORTION SPONTANEOUS ( 15 FDA reports)
AFFECT LABILITY ( 15 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 15 FDA reports)
ARTERIAL STENOSIS ( 15 FDA reports)
BLINDNESS TRANSIENT ( 15 FDA reports)
BLOOD LACTIC ACID INCREASED ( 15 FDA reports)
BLOOD PARATHYROID HORMONE INCREASED ( 15 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 15 FDA reports)
BODY TEMPERATURE ( 15 FDA reports)
CARBUNCLE ( 15 FDA reports)
CARDIAC DEATH ( 15 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 15 FDA reports)
CAROTID ARTERY OCCLUSION ( 15 FDA reports)
CATHETER REMOVAL ( 15 FDA reports)
COLORECTAL CANCER ( 15 FDA reports)
COMMUNICATION DISORDER ( 15 FDA reports)
CONCUSSION ( 15 FDA reports)
CORONARY ARTERY THROMBOSIS ( 15 FDA reports)
DENTAL PROSTHESIS USER ( 15 FDA reports)
DERMATITIS ACNEIFORM ( 15 FDA reports)
DYSPHASIA ( 15 FDA reports)
DYSPLASTIC NAEVUS ( 15 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 15 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 15 FDA reports)
FACET JOINT SYNDROME ( 15 FDA reports)
FOETAL GROWTH RESTRICTION ( 15 FDA reports)
GASTROINTESTINAL EROSION ( 15 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 15 FDA reports)
HAEMOGLOBIN ABNORMAL ( 15 FDA reports)
HAND DEFORMITY ( 15 FDA reports)
HEAD TITUBATION ( 15 FDA reports)
HERPES VIRUS INFECTION ( 15 FDA reports)
IMPETIGO ( 15 FDA reports)
INTESTINAL POLYP ( 15 FDA reports)
JAUNDICE CHOLESTATIC ( 15 FDA reports)
JOINT INSTABILITY ( 15 FDA reports)
KNEE OPERATION ( 15 FDA reports)
LIGAMENT RUPTURE ( 15 FDA reports)
MOOD ALTERED ( 15 FDA reports)
MULTIPLE FRACTURES ( 15 FDA reports)
MUSCLE RUPTURE ( 15 FDA reports)
MYOCARDITIS ( 15 FDA reports)
NON-SMALL CELL LUNG CANCER ( 15 FDA reports)
OPTIC ISCHAEMIC NEUROPATHY ( 15 FDA reports)
ADHESION ( 14 FDA reports)
ALCOHOLIC LIVER DISEASE ( 14 FDA reports)
ANAL FISSURE ( 14 FDA reports)
ANGIONEUROTIC OEDEMA ( 14 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 14 FDA reports)
AORTIC ANEURYSM RUPTURE ( 14 FDA reports)
APPETITE DISORDER ( 14 FDA reports)
ARTERIAL DISORDER ( 14 FDA reports)
AUTONOMIC NEUROPATHY ( 14 FDA reports)
BILIARY DILATATION ( 14 FDA reports)
BLADDER MASS ( 14 FDA reports)
BLOOD IRON DECREASED ( 14 FDA reports)
BLOOD OSMOLARITY DECREASED ( 14 FDA reports)
BONE ABSCESS ( 14 FDA reports)
BONE EROSION ( 14 FDA reports)
BRAIN MIDLINE SHIFT ( 14 FDA reports)
BRAIN NEOPLASM ( 14 FDA reports)
BREAST CANCER STAGE IV ( 14 FDA reports)
BREAST HYPERPLASIA ( 14 FDA reports)
CARDIAC ANEURYSM ( 14 FDA reports)
CARDIAC VALVE REPLACEMENT COMPLICATION ( 14 FDA reports)
CARDIOTOXICITY ( 14 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 14 FDA reports)
COLONIC HAEMATOMA ( 14 FDA reports)
COMPLEX PARTIAL SEIZURES ( 14 FDA reports)
DISEASE COMPLICATION ( 14 FDA reports)
DRUG SCREEN POSITIVE ( 14 FDA reports)
DYSCHEZIA ( 14 FDA reports)
DYSTONIA ( 14 FDA reports)
EAR CONGESTION ( 14 FDA reports)
EYE INFECTION ( 14 FDA reports)
EYE MOVEMENT DISORDER ( 14 FDA reports)
FEELING DRUNK ( 14 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 14 FDA reports)
FOOD INTOLERANCE ( 14 FDA reports)
FRACTURE NONUNION ( 14 FDA reports)
HEPATOCELLULAR INJURY ( 14 FDA reports)
HEPATOSPLENOMEGALY ( 14 FDA reports)
HYPERTENSIVE CRISIS ( 14 FDA reports)
IMMUNOSUPPRESSION ( 14 FDA reports)
IMPAIRED SELF-CARE ( 14 FDA reports)
INFERIOR VENA CAVAL OCCLUSION ( 14 FDA reports)
INJECTION SITE NODULE ( 14 FDA reports)
INTENTIONAL SELF-INJURY ( 14 FDA reports)
INTESTINAL INFARCTION ( 14 FDA reports)
LABELLED DRUG-DRUG INTERACTION MEDICATION ERROR ( 14 FDA reports)
MALIGNANT MELANOMA IN SITU ( 14 FDA reports)
MASTECTOMY ( 14 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 14 FDA reports)
MEDIASTINAL MASS ( 14 FDA reports)
METASTASES TO SPLEEN ( 14 FDA reports)
NEPHRITIC SYNDROME ( 14 FDA reports)
NODAL ARRHYTHMIA ( 14 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 14 FDA reports)
OEDEMA MUCOSAL ( 14 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 14 FDA reports)
OESOPHAGEAL STENOSIS ( 14 FDA reports)
OPTIC NERVE DISORDER ( 14 FDA reports)
ORAL FIBROMA ( 14 FDA reports)
OSTEOMYELITIS ACUTE ( 14 FDA reports)
OSTEOMYELITIS CHRONIC ( 14 FDA reports)
OVARIAN CANCER RECURRENT ( 14 FDA reports)
OXYGEN SUPPLEMENTATION ( 14 FDA reports)
PERITONITIS BACTERIAL ( 14 FDA reports)
PNEUMOCONIOSIS ( 14 FDA reports)
POLYCYTHAEMIA ( 14 FDA reports)
PROCEDURAL SITE REACTION ( 14 FDA reports)
PROTEIN TOTAL INCREASED ( 14 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 14 FDA reports)
PSYCHIATRIC SYMPTOM ( 14 FDA reports)
PULMONARY HILUM MASS ( 14 FDA reports)
RADIUS FRACTURE ( 14 FDA reports)
RASH PUSTULAR ( 14 FDA reports)
RENAL INFARCT ( 14 FDA reports)
RENAL MASS ( 14 FDA reports)
RENAL TUBULAR ACIDOSIS ( 14 FDA reports)
RESPIRATORY ALKALOSIS ( 14 FDA reports)
RETINOPATHY ( 14 FDA reports)
RHEUMATIC FEVER ( 14 FDA reports)
SCHIZOPHRENIA ( 14 FDA reports)
SCROTAL CYST ( 14 FDA reports)
SENSATION OF FOREIGN BODY ( 14 FDA reports)
SKIN INFECTION ( 14 FDA reports)
SPLENIC GRANULOMA ( 14 FDA reports)
SYSTEMIC SCLEROSIS ( 14 FDA reports)
TINEA CRURIS ( 14 FDA reports)
TONIC CONVULSION ( 14 FDA reports)
TOOTH DEPOSIT ( 14 FDA reports)
UMBILICAL HERNIA ( 14 FDA reports)
URETHRAL STENOSIS ( 14 FDA reports)
VARICES OESOPHAGEAL ( 14 FDA reports)
VASCULAR RUPTURE ( 14 FDA reports)
VERTIGO POSITIONAL ( 14 FDA reports)
VOCAL CORD DISORDER ( 14 FDA reports)
VOCAL CORD PARALYSIS ( 14 FDA reports)
WOUND COMPLICATION ( 14 FDA reports)
XANTHOPSIA ( 14 FDA reports)
PERIORBITAL OEDEMA ( 13 FDA reports)
POLYMYOSITIS ( 13 FDA reports)
PORTAL HYPERTENSION ( 13 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 13 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 13 FDA reports)
PULMONARY GRANULOMA ( 13 FDA reports)
PULSE ABNORMAL ( 13 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 13 FDA reports)
RADICULITIS CERVICAL ( 13 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 13 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 13 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 13 FDA reports)
RETINAL DISORDER ( 13 FDA reports)
SCREAMING ( 13 FDA reports)
SECONDARY SEQUESTRUM ( 13 FDA reports)
SEXUAL DYSFUNCTION ( 13 FDA reports)
SKIN EROSION ( 13 FDA reports)
SKIN FISSURES ( 13 FDA reports)
THYROID CANCER ( 13 FDA reports)
THYROIDITIS ( 13 FDA reports)
TUMOUR INVASION ( 13 FDA reports)
URINE OUTPUT INCREASED ( 13 FDA reports)
UTERINE LEIOMYOMA ( 13 FDA reports)
VENTRICULAR FAILURE ( 13 FDA reports)
VITAMIN D DECREASED ( 13 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 13 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 13 FDA reports)
WOUND DEBRIDEMENT ( 13 FDA reports)
AKINESIA ( 13 FDA reports)
AORTIC DILATATION ( 13 FDA reports)
APPLICATION SITE ERYTHEMA ( 13 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 13 FDA reports)
AUTOIMMUNE HEPATITIS ( 13 FDA reports)
BACTERIAL SEPSIS ( 13 FDA reports)
BLOOD BICARBONATE DECREASED ( 13 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 13 FDA reports)
BONE CALLUS EXCESSIVE ( 13 FDA reports)
BONE FISSURE ( 13 FDA reports)
BREAST TENDERNESS ( 13 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 13 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 13 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 13 FDA reports)
CYSTOSCOPY ( 13 FDA reports)
DEMENTIA WITH LEWY BODIES ( 13 FDA reports)
DERMAL CYST ( 13 FDA reports)
DERMATOPHYTOSIS ( 13 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 13 FDA reports)
EROSIVE DUODENITIS ( 13 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 13 FDA reports)
EXTRASKELETAL OSSIFICATION ( 13 FDA reports)
EYE OEDEMA ( 13 FDA reports)
FEMALE STERILISATION ( 13 FDA reports)
FLAT AFFECT ( 13 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 13 FDA reports)
GUN SHOT WOUND ( 13 FDA reports)
HAEMOGLOBIN INCREASED ( 13 FDA reports)
HALLUCINATION, AUDITORY ( 13 FDA reports)
HEPATIC FIBROSIS ( 13 FDA reports)
HYPERAESTHESIA ( 13 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 13 FDA reports)
HYPOPROTEINAEMIA ( 13 FDA reports)
INFECTIOUS PERITONITIS ( 13 FDA reports)
INTERVERTEBRAL DISCITIS ( 13 FDA reports)
LIP DRY ( 13 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 13 FDA reports)
MACROCYTOSIS ( 13 FDA reports)
MALABSORPTION ( 13 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 13 FDA reports)
MENIERE'S DISEASE ( 13 FDA reports)
METASTASES TO CHEST WALL ( 13 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 13 FDA reports)
OBSTRUCTION GASTRIC ( 13 FDA reports)
OCCULT BLOOD ( 13 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 13 FDA reports)
OPERATIVE HAEMORRHAGE ( 13 FDA reports)
ORAL MUCOSA EROSION ( 13 FDA reports)
PARKINSONISM ( 13 FDA reports)
PCO2 DECREASED ( 13 FDA reports)
PERFORMANCE STATUS DECREASED ( 13 FDA reports)
ADENOMYOSIS ( 12 FDA reports)
ADRENAL ADENOMA ( 12 FDA reports)
ALCOHOLISM ( 12 FDA reports)
AMYLOIDOSIS ( 12 FDA reports)
ANOSMIA ( 12 FDA reports)
ANXIETY DISORDER ( 12 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 12 FDA reports)
AUTOIMMUNE DISORDER ( 12 FDA reports)
BILIARY COLIC ( 12 FDA reports)
BLADDER NEOPLASM ( 12 FDA reports)
BLOOD VISCOSITY INCREASED ( 12 FDA reports)
BONE DEFORMITY ( 12 FDA reports)
BOWEL SOUNDS ABNORMAL ( 12 FDA reports)
BREAST CYST ( 12 FDA reports)
BRONCHIAL CARCINOMA ( 12 FDA reports)
CAPILLARY LEAK SYNDROME ( 12 FDA reports)
CARDIORENAL SYNDROME ( 12 FDA reports)
CATATONIA ( 12 FDA reports)
CATHETER SITE INFECTION ( 12 FDA reports)
CHOLECYSTITIS INFECTIVE ( 12 FDA reports)
COLPOCELE ( 12 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 12 FDA reports)
CRANIAL NERVE DISORDER ( 12 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 12 FDA reports)
EFFUSION ( 12 FDA reports)
EJECTION FRACTION ABNORMAL ( 12 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 12 FDA reports)
EYELID PTOSIS ( 12 FDA reports)
FOLATE DEFICIENCY ( 12 FDA reports)
FULL BLOOD COUNT DECREASED ( 12 FDA reports)
GALLBLADDER ENLARGEMENT ( 12 FDA reports)
HAEMATOCRIT INCREASED ( 12 FDA reports)
HEART SOUNDS ABNORMAL ( 12 FDA reports)
HERNIA REPAIR ( 12 FDA reports)
HYPERKINESIA ( 12 FDA reports)
HYPERPARATHYROIDISM ( 12 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 12 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 12 FDA reports)
INHIBITORY DRUG INTERACTION ( 12 FDA reports)
INJECTION SITE INFECTION ( 12 FDA reports)
INTESTINAL HAEMATOMA ( 12 FDA reports)
JOINT ARTHROPLASTY ( 12 FDA reports)
KETOSIS ( 12 FDA reports)
LHERMITTE'S SIGN ( 12 FDA reports)
LIGAMENT INJURY ( 12 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 12 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 12 FDA reports)
MIOSIS ( 12 FDA reports)
MULTI-ORGAN DISORDER ( 12 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 12 FDA reports)
NASAL DISCOMFORT ( 12 FDA reports)
NASAL POLYPS ( 12 FDA reports)
NOCTURNAL DYSPNOEA ( 12 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 12 FDA reports)
OLFACTORY NERVE DISORDER ( 12 FDA reports)
ORAL HERPES ( 12 FDA reports)
OSTEOMA ( 12 FDA reports)
OVARIAN CANCER ( 12 FDA reports)
PANCREATIC DISORDER ( 12 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 12 FDA reports)
PHARYNGEAL ERYTHEMA ( 12 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 12 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 12 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 12 FDA reports)
PULMONARY TUBERCULOSIS ( 12 FDA reports)
PULSE PRESSURE DECREASED ( 12 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 12 FDA reports)
PUPILS UNEQUAL ( 12 FDA reports)
RECTAL CANCER ( 12 FDA reports)
RECURRENT CANCER ( 12 FDA reports)
RENAL EMBOLISM ( 12 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 12 FDA reports)
SCROTAL OEDEMA ( 12 FDA reports)
SEROMA ( 12 FDA reports)
SERRATIA INFECTION ( 12 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 12 FDA reports)
SOMNAMBULISM ( 12 FDA reports)
SPLENIC RUPTURE ( 12 FDA reports)
STUPOR ( 12 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 12 FDA reports)
SYSTEMIC CANDIDA ( 12 FDA reports)
THERMAL BURN ( 12 FDA reports)
THROMBOCYTHAEMIA ( 12 FDA reports)
TOE AMPUTATION ( 12 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 12 FDA reports)
TRIGEMINAL NEURALGIA ( 12 FDA reports)
VAGINAL PROLAPSE ( 12 FDA reports)
VASCULAR INSUFFICIENCY ( 12 FDA reports)
VENA CAVA FILTER INSERTION ( 12 FDA reports)
VITREOUS DETACHMENT ( 12 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 12 FDA reports)
PERIORBITAL HAEMATOMA ( 11 FDA reports)
PROCTALGIA ( 11 FDA reports)
PROTEIN S DEFICIENCY ( 11 FDA reports)
PROTEUS INFECTION ( 11 FDA reports)
PULMONARY ARTERIAL PRESSURE DECREASED ( 11 FDA reports)
RENAL VEIN THROMBOSIS ( 11 FDA reports)
RETINAL VEIN OCCLUSION ( 11 FDA reports)
RHEUMATIC HEART DISEASE ( 11 FDA reports)
RHEUMATOID NODULE ( 11 FDA reports)
SARCOIDOSIS ( 11 FDA reports)
SOFT TISSUE NECROSIS ( 11 FDA reports)
SPINAL CORD HAEMORRHAGE ( 11 FDA reports)
SPINAL EPIDURAL HAEMORRHAGE ( 11 FDA reports)
SYMPATHETIC POSTERIOR CERVICAL SYNDROME ( 11 FDA reports)
TANDEM GAIT TEST ABNORMAL ( 11 FDA reports)
TENSION ( 11 FDA reports)
THYROIDECTOMY ( 11 FDA reports)
TONGUE HAEMORRHAGE ( 11 FDA reports)
TOOTH REPAIR ( 11 FDA reports)
TOURETTE'S DISORDER ( 11 FDA reports)
TOXIC ENCEPHALOPATHY ( 11 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 11 FDA reports)
URGE INCONTINENCE ( 11 FDA reports)
URINARY TRACT OBSTRUCTION ( 11 FDA reports)
URINE COLOUR ABNORMAL ( 11 FDA reports)
VASCULAR GRAFT OCCLUSION ( 11 FDA reports)
VITAMIN B12 DEFICIENCY ( 11 FDA reports)
VULVOVAGINITIS ( 11 FDA reports)
ABDOMINAL RIGIDITY ( 11 FDA reports)
ADJUSTMENT DISORDER ( 11 FDA reports)
AKATHISIA ( 11 FDA reports)
ALKALOSIS HYPOKALAEMIC ( 11 FDA reports)
AORTIC VALVE REPLACEMENT ( 11 FDA reports)
ARTHRITIS INFECTIVE ( 11 FDA reports)
ASPERGILLOSIS ( 11 FDA reports)
ASPIRATION PLEURAL CAVITY ( 11 FDA reports)
AXILLARY VEIN THROMBOSIS ( 11 FDA reports)
BACTERIAL TEST POSITIVE ( 11 FDA reports)
BARTHOLIN'S CYST ( 11 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 11 FDA reports)
BASEDOW'S DISEASE ( 11 FDA reports)
BLOOD PH INCREASED ( 11 FDA reports)
BLOOD UREA ABNORMAL ( 11 FDA reports)
BONE GIANT CELL TUMOUR ( 11 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 11 FDA reports)
CATHETER SITE PAIN ( 11 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 11 FDA reports)
CHEST TUBE INSERTION ( 11 FDA reports)
CHORIORETINOPATHY ( 11 FDA reports)
COMA SCALE ABNORMAL ( 11 FDA reports)
CULTURE WOUND POSITIVE ( 11 FDA reports)
CUTANEOUS VASCULITIS ( 11 FDA reports)
CYSTITIS HAEMORRHAGIC ( 11 FDA reports)
CYTOLYTIC HEPATITIS ( 11 FDA reports)
DRUG ABUSE ( 11 FDA reports)
DRY THROAT ( 11 FDA reports)
DUODENAL ULCER PERFORATION ( 11 FDA reports)
DYSGRAPHIA ( 11 FDA reports)
ENGRAFTMENT SYNDROME ( 11 FDA reports)
FISTULA DISCHARGE ( 11 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 11 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 11 FDA reports)
GLOMERULONEPHRITIS ( 11 FDA reports)
HAEMORRHAGIC CYST ( 11 FDA reports)
HEARING DISABILITY ( 11 FDA reports)
HEART DISEASE CONGENITAL ( 11 FDA reports)
HEPATIC HAEMORRHAGE ( 11 FDA reports)
HEPATOJUGULAR REFLUX ( 11 FDA reports)
HICCUPS ( 11 FDA reports)
HIP SURGERY ( 11 FDA reports)
HYPERTONIA ( 11 FDA reports)
HYPERTONIC BLADDER ( 11 FDA reports)
HYPOGONADISM ( 11 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 11 FDA reports)
INJECTION SITE DISCOLOURATION ( 11 FDA reports)
INJECTION SITE INDURATION ( 11 FDA reports)
INTESTINAL STENOSIS ( 11 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 11 FDA reports)
KERATITIS ( 11 FDA reports)
LIP HAEMORRHAGE ( 11 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 11 FDA reports)
LUNG HYPERINFLATION ( 11 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 11 FDA reports)
MACROGLOSSIA ( 11 FDA reports)
METASTASES TO BONE MARROW ( 11 FDA reports)
MUCOSAL HAEMORRHAGE ( 11 FDA reports)
NASAL ULCER ( 11 FDA reports)
NEPHRITIS ( 11 FDA reports)
OCCIPITAL NEURALGIA ( 11 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 11 FDA reports)
OROANTRAL FISTULA ( 11 FDA reports)
ORTHOSIS USER ( 11 FDA reports)
PANIC REACTION ( 11 FDA reports)
PARESIS ( 11 FDA reports)
PEAU D'ORANGE ( 11 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 10 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 10 FDA reports)
ANION GAP INCREASED ( 10 FDA reports)
ARTERIAL HAEMORRHAGE ( 10 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 10 FDA reports)
BONE MARROW DISORDER ( 10 FDA reports)
BONE MARROW TOXICITY ( 10 FDA reports)
BRAIN SCAN ABNORMAL ( 10 FDA reports)
BRAIN STEM INFARCTION ( 10 FDA reports)
CEREBELLAR INFARCTION ( 10 FDA reports)
CHOLESTATIC LIVER INJURY ( 10 FDA reports)
CHOLESTEATOMA ( 10 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 10 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 10 FDA reports)
COMA HEPATIC ( 10 FDA reports)
CONNECTIVE TISSUE DISORDER ( 10 FDA reports)
CONVERSION DISORDER ( 10 FDA reports)
CYTOKINE STORM ( 10 FDA reports)
DENTAL ALVEOLAR ANOMALY ( 10 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 10 FDA reports)
DRUG LEVEL CHANGED ( 10 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 10 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 10 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 10 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 10 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 10 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 10 FDA reports)
ENTEROVESICAL FISTULA ( 10 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 10 FDA reports)
EYE DISCHARGE ( 10 FDA reports)
EYE ROLLING ( 10 FDA reports)
FEEDING DISORDER ( 10 FDA reports)
FOAMING AT MOUTH ( 10 FDA reports)
FOETAL WARFARIN SYNDROME ( 10 FDA reports)
GAMMOPATHY ( 10 FDA reports)
GASTRECTOMY ( 10 FDA reports)
GENITAL HERPES ( 10 FDA reports)
GLOMERULAR FILTRATION RATE ABNORMAL ( 10 FDA reports)
GLOMERULONEPHRITIS MEMBRANOUS ( 10 FDA reports)
GOUTY ARTHRITIS ( 10 FDA reports)
HOMICIDAL IDEATION ( 10 FDA reports)
HORDEOLUM ( 10 FDA reports)
HYPOCHLORAEMIA ( 10 FDA reports)
ILEOSTOMY ( 10 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 10 FDA reports)
INGUINAL HERNIA REPAIR ( 10 FDA reports)
JOINT LOCK ( 10 FDA reports)
KLEBSIELLA BACTERAEMIA ( 10 FDA reports)
KYPHOSCOLIOSIS ( 10 FDA reports)
LAGOPHTHALMOS ( 10 FDA reports)
LUMBAR RADICULOPATHY ( 10 FDA reports)
LUNG ADENOCARCINOMA ( 10 FDA reports)
MALIGNANT TUMOUR EXCISION ( 10 FDA reports)
MASS EXCISION ( 10 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 10 FDA reports)
MULTIPLE ALLERGIES ( 10 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 10 FDA reports)
NAIL DISCOLOURATION ( 10 FDA reports)
NEOPLASM RECURRENCE ( 10 FDA reports)
NERVE ROOT COMPRESSION ( 10 FDA reports)
NEUROGENIC BLADDER ( 10 FDA reports)
NEUTROPHILIA ( 10 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 10 FDA reports)
NOSOCOMIAL INFECTION ( 10 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 10 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 10 FDA reports)
OVARIAN HAEMORRHAGE ( 10 FDA reports)
PAINFUL RESPIRATION ( 10 FDA reports)
PARAPROTEINAEMIA ( 10 FDA reports)
PATHOGEN RESISTANCE ( 10 FDA reports)
PATHOLOGICAL GAMBLING ( 10 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 10 FDA reports)
PNEUMONIA FUNGAL ( 10 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 10 FDA reports)
PNEUMOTHORAX SPONTANEOUS TENSION ( 10 FDA reports)
PRIAPISM ( 10 FDA reports)
PROSTATE INFECTION ( 10 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 10 FDA reports)
RADIOTHERAPY TO BRAIN ( 10 FDA reports)
RENAL HAEMATOMA ( 10 FDA reports)
RETICULOCYTE COUNT INCREASED ( 10 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 10 FDA reports)
SKELETAL INJURY ( 10 FDA reports)
SKIN REACTION ( 10 FDA reports)
SOPOR ( 10 FDA reports)
SPINAL X-RAY ABNORMAL ( 10 FDA reports)
STENT OCCLUSION ( 10 FDA reports)
TEARFULNESS ( 10 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 10 FDA reports)
TRANSPLANT REJECTION ( 10 FDA reports)
VAGINAL INFECTION ( 10 FDA reports)
VASODILATATION ( 10 FDA reports)
VERTEBRAL WEDGING ( 10 FDA reports)
VISUAL BRIGHTNESS ( 10 FDA reports)
WOUND DRAINAGE ( 10 FDA reports)
PITUITARY TUMOUR ( 9 FDA reports)
POLYARTHRITIS ( 9 FDA reports)
POLYPECTOMY ( 9 FDA reports)
POOR VENOUS ACCESS ( 9 FDA reports)
POST PROCEDURAL INFECTION ( 9 FDA reports)
POSTNASAL DRIP ( 9 FDA reports)
POSTOPERATIVE INFECTION ( 9 FDA reports)
PROCEDURAL HYPOTENSION ( 9 FDA reports)
PROSTATE CANCER METASTATIC ( 9 FDA reports)
PULMONARY VASCULAR DISORDER ( 9 FDA reports)
RADIATION SKIN INJURY ( 9 FDA reports)
RASH VESICULAR ( 9 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 9 FDA reports)
SEPSIS SYNDROME ( 9 FDA reports)
SLEEP TALKING ( 9 FDA reports)
SNORING ( 9 FDA reports)
SOFT TISSUE INFECTION ( 9 FDA reports)
SPLENIC VEIN THROMBOSIS ( 9 FDA reports)
STREPTOCOCCAL SEPSIS ( 9 FDA reports)
STRIDOR ( 9 FDA reports)
SURGICAL PROCEDURE REPEATED ( 9 FDA reports)
TEMPORAL LOBE EPILEPSY ( 9 FDA reports)
TENDON GRAFT ( 9 FDA reports)
TERATOMA ( 9 FDA reports)
TONGUE BITING ( 9 FDA reports)
TONGUE OEDEMA ( 9 FDA reports)
TOOTH DISCOLOURATION ( 9 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 9 FDA reports)
TRAUMATIC HAEMATOMA ( 9 FDA reports)
TUMOUR MARKER INCREASED ( 9 FDA reports)
TYPE 1 DIABETES MELLITUS ( 9 FDA reports)
URETHRITIS ( 9 FDA reports)
UTERINE POLYP ( 9 FDA reports)
VASCULAR DEMENTIA ( 9 FDA reports)
VASCULITIC RASH ( 9 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 9 FDA reports)
VULVAL DISORDER ( 9 FDA reports)
WEANING FAILURE ( 9 FDA reports)
ABDOMINAL WALL INFECTION ( 9 FDA reports)
ABSCESS ORAL ( 9 FDA reports)
ACUTE ABDOMEN ( 9 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 9 FDA reports)
ALCOHOL ABUSE ( 9 FDA reports)
ALVEOLITIS ALLERGIC ( 9 FDA reports)
AMMONIA INCREASED ( 9 FDA reports)
AMPUTATION ( 9 FDA reports)
ANASTOMOTIC COMPLICATION ( 9 FDA reports)
ANIMAL BITE ( 9 FDA reports)
ANTICOAGULANT THERAPY ( 9 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 9 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 9 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 9 FDA reports)
APPENDICECTOMY ( 9 FDA reports)
APPLICATION SITE PAIN ( 9 FDA reports)
ARTHROSCOPIC SURGERY ( 9 FDA reports)
ASEPTIC NECROSIS BONE ( 9 FDA reports)
AXILLARY MASS ( 9 FDA reports)
BETA GLOBULIN INCREASED ( 9 FDA reports)
BIOPSY SKIN ABNORMAL ( 9 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 9 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 9 FDA reports)
BOVINE TUBERCULOSIS ( 9 FDA reports)
BURNS THIRD DEGREE ( 9 FDA reports)
CARDIAC PROCEDURE COMPLICATION ( 9 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 9 FDA reports)
CARTILAGE ATROPHY ( 9 FDA reports)
CATHETER SITE RELATED REACTION ( 9 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 9 FDA reports)
CHANGE OF BOWEL HABIT ( 9 FDA reports)
CHROMATOPSIA ( 9 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 9 FDA reports)
CLAVICLE FRACTURE ( 9 FDA reports)
COLITIS MICROSCOPIC ( 9 FDA reports)
COLONIC PSEUDO-OBSTRUCTION ( 9 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 9 FDA reports)
CORONARY ARTERY SURGERY ( 9 FDA reports)
DEEP VEIN THROMBOSIS POSTOPERATIVE ( 9 FDA reports)
DENTAL PLAQUE ( 9 FDA reports)
DYSLALIA ( 9 FDA reports)
EMPYEMA ( 9 FDA reports)
ENTERITIS ( 9 FDA reports)
ENTERITIS INFECTIOUS ( 9 FDA reports)
ENTEROBACTER INFECTION ( 9 FDA reports)
EOSINOPHILIC PNEUMONIA ( 9 FDA reports)
ESCHERICHIA SEPSIS ( 9 FDA reports)
EXOPHTHALMOS ( 9 FDA reports)
FACET JOINT BLOCK ( 9 FDA reports)
FASCIITIS ( 9 FDA reports)
FAT NECROSIS ( 9 FDA reports)
GASTRITIS ATROPHIC ( 9 FDA reports)
GINGIVAL ATROPHY ( 9 FDA reports)
H1N1 INFLUENZA ( 9 FDA reports)
HAEMORRHAGIC ASCITES ( 9 FDA reports)
HAEMORRHAGIC DISORDER ( 9 FDA reports)
HEART TRANSPLANT ( 9 FDA reports)
HEAT RASH ( 9 FDA reports)
HEPATIC HAEMATOMA ( 9 FDA reports)
HEPATIC INFARCTION ( 9 FDA reports)
HEPATIC NECROSIS ( 9 FDA reports)
HEPATOCELLULAR DAMAGE ( 9 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 9 FDA reports)
HOSTILITY ( 9 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 9 FDA reports)
IMMUNE SYSTEM DISORDER ( 9 FDA reports)
INJECTION SITE RASH ( 9 FDA reports)
INTESTINAL ULCER ( 9 FDA reports)
INTRA-UTERINE DEATH ( 9 FDA reports)
KERATOPATHY ( 9 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 9 FDA reports)
LABORATORY TEST INTERFERENCE ( 9 FDA reports)
LIBIDO DECREASED ( 9 FDA reports)
LIFE SUPPORT ( 9 FDA reports)
LIVER ABSCESS ( 9 FDA reports)
LOSS OF BLADDER SENSATION ( 9 FDA reports)
MACULAR OEDEMA ( 9 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 9 FDA reports)
METAMORPHOPSIA ( 9 FDA reports)
METASTASES TO THE MEDIASTINUM ( 9 FDA reports)
METATARSALGIA ( 9 FDA reports)
MICROANGIOPATHY ( 9 FDA reports)
MICROCYTIC ANAEMIA ( 9 FDA reports)
MITRAL VALVE REPAIR ( 9 FDA reports)
MITRAL VALVE REPLACEMENT ( 9 FDA reports)
MOANING ( 9 FDA reports)
MONONEURITIS ( 9 FDA reports)
MORTON'S NEUROMA ( 9 FDA reports)
MUSCLE FATIGUE ( 9 FDA reports)
MYASTHENIA GRAVIS ( 9 FDA reports)
MYELITIS TRANSVERSE ( 9 FDA reports)
MYOCARDIAL FIBROSIS ( 9 FDA reports)
NEPHRITIS ALLERGIC ( 9 FDA reports)
NEUROPATHIC ULCER ( 9 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 9 FDA reports)
NONSPECIFIC REACTION ( 9 FDA reports)
OBSTRUCTION ( 9 FDA reports)
OEDEMA GENITAL ( 9 FDA reports)
OESOPHAGEAL CARCINOMA ( 9 FDA reports)
OESOPHAGEAL DISORDER ( 9 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 9 FDA reports)
OPTIC NEUROPATHY ( 9 FDA reports)
OTITIS MEDIA ACUTE ( 9 FDA reports)
PANIC DISORDER ( 9 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 8 FDA reports)
ACUTE SINUSITIS ( 8 FDA reports)
ALDOLASE INCREASED ( 8 FDA reports)
ANGIOPLASTY ( 8 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 8 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 8 FDA reports)
APLASTIC ANAEMIA ( 8 FDA reports)
APPENDICITIS ( 8 FDA reports)
APPLICATION SITE IRRITATION ( 8 FDA reports)
ARTERIAL INJURY ( 8 FDA reports)
ARTERIOVENOUS FISTULA SITE HAEMORRHAGE ( 8 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 8 FDA reports)
ARTHROPOD BITE ( 8 FDA reports)
AXONAL NEUROPATHY ( 8 FDA reports)
B-CELL LYMPHOMA ( 8 FDA reports)
BENCE JONES PROTEINURIA ( 8 FDA reports)
BILE DUCT CANCER ( 8 FDA reports)
BIOPSY BLADDER ABNORMAL ( 8 FDA reports)
BLADDER NECK OPERATION ( 8 FDA reports)
BLADDER PERFORATION ( 8 FDA reports)
BLEPHAROSPASM ( 8 FDA reports)
BLOOD BICARBONATE INCREASED ( 8 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 8 FDA reports)
BLOOD MAGNESIUM INCREASED ( 8 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 8 FDA reports)
BONE MARROW GRANULOMA ( 8 FDA reports)
BRAIN MASS ( 8 FDA reports)
BREAST CALCIFICATIONS ( 8 FDA reports)
BRONCHIAL SECRETION RETENTION ( 8 FDA reports)
BRONCHIOLITIS ( 8 FDA reports)
CARBON DIOXIDE INCREASED ( 8 FDA reports)
CARDIAC ABLATION ( 8 FDA reports)
CEREBRAL MICROANGIOPATHY ( 8 FDA reports)
CHALAZION ( 8 FDA reports)
CHONDROCALCINOSIS PYROPHOSPHATE ( 8 FDA reports)
CHORIORETINAL DISORDER ( 8 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 8 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 8 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 8 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 8 FDA reports)
COCCIDIOIDOMYCOSIS ( 8 FDA reports)
COLLAGEN DISORDER ( 8 FDA reports)
COLON CANCER METASTATIC ( 8 FDA reports)
COLONIC OBSTRUCTION ( 8 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 8 FDA reports)
CORNEAL DISORDER ( 8 FDA reports)
CORNEAL OPERATION ( 8 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 8 FDA reports)
CYSTOPEXY ( 8 FDA reports)
DANDY-WALKER SYNDROME ( 8 FDA reports)
DEMYELINATION ( 8 FDA reports)
DERMOID CYST ( 8 FDA reports)
DIABETIC MICROANGIOPATHY ( 8 FDA reports)
DIET REFUSAL ( 8 FDA reports)
DIVERTICULAR PERFORATION ( 8 FDA reports)
ENCEPHALOMALACIA ( 8 FDA reports)
ENURESIS ( 8 FDA reports)
ESCHERICHIA BACTERAEMIA ( 8 FDA reports)
EUSTACHIAN TUBE DYSFUNCTION ( 8 FDA reports)
EYE LASER SURGERY ( 8 FDA reports)
FAECES PALE ( 8 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 8 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 8 FDA reports)
GASTRIC ANTRAL VASCULAR ECTASIA ( 8 FDA reports)
GASTRIC CANCER RECURRENT ( 8 FDA reports)
GASTRIC MUCOSAL LESION ( 8 FDA reports)
GASTRIC OPERATION ( 8 FDA reports)
GASTRIC PERFORATION ( 8 FDA reports)
GASTROINTESTINAL CARCINOMA ( 8 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 8 FDA reports)
GINGIVAL HYPERPLASIA ( 8 FDA reports)
GLUCOSE URINE PRESENT ( 8 FDA reports)
GRANULOCYTE COUNT DECREASED ( 8 FDA reports)
HAEMATOMA EVACUATION ( 8 FDA reports)
HAIR FOLLICLE TUMOUR BENIGN ( 8 FDA reports)
HALO VISION ( 8 FDA reports)
HEAD DISCOMFORT ( 8 FDA reports)
HELICOBACTER TEST POSITIVE ( 8 FDA reports)
HEPATIC ATROPHY ( 8 FDA reports)
HEPATIC ENZYME ABNORMAL ( 8 FDA reports)
HEPATIC TRAUMA ( 8 FDA reports)
HEREDITARY ANGIOEDEMA ( 8 FDA reports)
HIGH FREQUENCY ABLATION ( 8 FDA reports)
HYPERAMMONAEMIC ENCEPHALOPATHY ( 8 FDA reports)
HYPERHOMOCYSTEINAEMIA ( 8 FDA reports)
HYPERMAGNESAEMIA ( 8 FDA reports)
HYPERMETABOLISM ( 8 FDA reports)
HYPOPERFUSION ( 8 FDA reports)
HYPOTRICHOSIS ( 8 FDA reports)
ILIAC ARTERY THROMBOSIS ( 8 FDA reports)
IMPLANT SITE THROMBOSIS ( 8 FDA reports)
INCREASED BRONCHIAL SECRETION ( 8 FDA reports)
INJECTION SITE MASS ( 8 FDA reports)
IRON DEFICIENCY ( 8 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 8 FDA reports)
LARGE INTESTINE CARCINOMA ( 8 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 8 FDA reports)
LIP PAIN ( 8 FDA reports)
LOSS OF CONTROL OF LEGS ( 8 FDA reports)
MARROW HYPERPLASIA ( 8 FDA reports)
MEAN CELL VOLUME INCREASED ( 8 FDA reports)
MEGAKARYOCYTES INCREASED ( 8 FDA reports)
MENINGITIS MENINGOCOCCAL ( 8 FDA reports)
MERALGIA PARAESTHETICA ( 8 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 8 FDA reports)
MIDDLE EAR EFFUSION ( 8 FDA reports)
MONARTHRITIS ( 8 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 8 FDA reports)
MUSCLE SWELLING ( 8 FDA reports)
MYOPATHY TOXIC ( 8 FDA reports)
NEUTROPENIC COLITIS ( 8 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 8 FDA reports)
OESOPHAGEAL HYPOMOTILITY ( 8 FDA reports)
OESOPHAGEAL SPASM ( 8 FDA reports)
ORAL SOFT TISSUE DISORDER ( 8 FDA reports)
OROPHARYNGEAL BLISTERING ( 8 FDA reports)
PANCREATIC PSEUDOCYST ( 8 FDA reports)
PCO2 INCREASED ( 8 FDA reports)
PELVIC MASS ( 8 FDA reports)
PERIPHERAL NERVE INJURY ( 8 FDA reports)
PHARYNGEAL ABSCESS ( 8 FDA reports)
PHARYNGEAL DISORDER ( 8 FDA reports)
PHARYNGEAL HAEMATOMA ( 8 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 8 FDA reports)
PLASMACYTOSIS ( 8 FDA reports)
PNEUMONIA VIRAL ( 8 FDA reports)
POST PROCEDURAL PAIN ( 8 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 8 FDA reports)
PROTEIN C DECREASED ( 8 FDA reports)
PRURITUS GENITAL ( 8 FDA reports)
PULMONARY CALCIFICATION ( 8 FDA reports)
PUTAMEN HAEMORRHAGE ( 8 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 8 FDA reports)
REGURGITATION ( 8 FDA reports)
RETINAL SCAR ( 8 FDA reports)
SHOULDER ARTHROPLASTY ( 8 FDA reports)
SINUS OPERATION ( 8 FDA reports)
SKIN NEOPLASM EXCISION ( 8 FDA reports)
SKIN OEDEMA ( 8 FDA reports)
SOFT TISSUE DISORDER ( 8 FDA reports)
STENOTROPHOMONAS INFECTION ( 8 FDA reports)
SUBCUTANEOUS NODULE ( 8 FDA reports)
SUTURE RELATED COMPLICATION ( 8 FDA reports)
TENSION HEADACHE ( 8 FDA reports)
TERMINAL STATE ( 8 FDA reports)
TESTICULAR MASS ( 8 FDA reports)
THALAMIC INFARCTION ( 8 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 8 FDA reports)
TONGUE COATED ( 8 FDA reports)
URINARY TRACT NEOPLASM ( 8 FDA reports)
UTERINE CANCER ( 8 FDA reports)
VASCULAR GRAFT ( 8 FDA reports)
VASOSPASM ( 8 FDA reports)
VENOUS STASIS ( 8 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 8 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 8 FDA reports)
WHITE BLOOD CELL DISORDER ( 8 FDA reports)
PERITONEAL DIALYSIS ( 7 FDA reports)
PHOBIA ( 7 FDA reports)
PHYSIOTHERAPY ( 7 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 7 FDA reports)
POLYTRAUMATISM ( 7 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 7 FDA reports)
POSTOPERATIVE WOUND COMPLICATION ( 7 FDA reports)
PROCTITIS ( 7 FDA reports)
PRODUCT MEASURED POTENCY ISSUE ( 7 FDA reports)
PROSTATE CANCER STAGE IV ( 7 FDA reports)
PROSTATIC DISORDER ( 7 FDA reports)
RADIATION INJURY ( 7 FDA reports)
READING DISORDER ( 7 FDA reports)
RENAL COLIC ( 7 FDA reports)
RENAL LIPOMATOSIS ( 7 FDA reports)
RENAL TRANSPLANT ( 7 FDA reports)
RESPIRATION ABNORMAL ( 7 FDA reports)
RETICULOCYTE COUNT DECREASED ( 7 FDA reports)
RETINAL EXUDATES ( 7 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 7 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 7 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 7 FDA reports)
SKIN TURGOR DECREASED ( 7 FDA reports)
SPINAL DEFORMITY ( 7 FDA reports)
STERNAL FRACTURE ( 7 FDA reports)
STREPTOCOCCUS TEST POSITIVE ( 7 FDA reports)
STRESS CARDIOMYOPATHY ( 7 FDA reports)
STRESS ULCER ( 7 FDA reports)
SUDDEN ONSET OF SLEEP ( 7 FDA reports)
SYNCOPE VASOVAGAL ( 7 FDA reports)
TENDON INJURY ( 7 FDA reports)
THALAMUS HAEMORRHAGE ( 7 FDA reports)
TONGUE HAEMATOMA ( 7 FDA reports)
TRAUMATIC LUNG INJURY ( 7 FDA reports)
TROPONIN T INCREASED ( 7 FDA reports)
TUMOUR NECROSIS ( 7 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 7 FDA reports)
UNEMPLOYMENT ( 7 FDA reports)
URETERAL DISORDER ( 7 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 7 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 7 FDA reports)
VAGOTOMY ( 7 FDA reports)
VASCULAR BYPASS GRAFT ( 7 FDA reports)
VENOUS INJURY ( 7 FDA reports)
VERTEBRAL COLUMN MASS ( 7 FDA reports)
VITAMIN B1 INCREASED ( 7 FDA reports)
WEIGHT BEARING DIFFICULTY ( 7 FDA reports)
WOUND NECROSIS ( 7 FDA reports)
ABDOMINAL INJURY ( 7 FDA reports)
ABNORMAL SENSATION IN EYE ( 7 FDA reports)
ABSCESS NECK ( 7 FDA reports)
ACIDOSIS HYPERCHLORAEMIC ( 7 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 7 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 7 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 7 FDA reports)
ADENOCARCINOMA ( 7 FDA reports)
ADENOMA BENIGN ( 7 FDA reports)
AGE-RELATED MACULAR DEGENERATION ( 7 FDA reports)
ALCOHOL INTERACTION ( 7 FDA reports)
ALCOHOL POISONING ( 7 FDA reports)
ALCOHOL WITHDRAWAL SYNDROME ( 7 FDA reports)
ALVEOLITIS ( 7 FDA reports)
ANORECTAL DISORDER ( 7 FDA reports)
ARM AMPUTATION ( 7 FDA reports)
ARTERIOGRAM CORONARY ABNORMAL ( 7 FDA reports)
ASPERGILLOMA ( 7 FDA reports)
ATHEROSCLEROSIS ( 7 FDA reports)
AUTOIMMUNE NEUTROPENIA ( 7 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 7 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 7 FDA reports)
BILE DUCT OBSTRUCTION ( 7 FDA reports)
BILE DUCT STONE ( 7 FDA reports)
BIOPSY BONE ABNORMAL ( 7 FDA reports)
BLOOD CREATININE DECREASED ( 7 FDA reports)
BLOOD IRON INCREASED ( 7 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 7 FDA reports)
BONE SARCOMA ( 7 FDA reports)
BRADYKINESIA ( 7 FDA reports)
BRADYPHRENIA ( 7 FDA reports)
BRAIN ABSCESS ( 7 FDA reports)
BREAST HAEMATOMA ( 7 FDA reports)
BREAST SWELLING ( 7 FDA reports)
BURNS SECOND DEGREE ( 7 FDA reports)
CALCULUS URETERIC ( 7 FDA reports)
CANDIDURIA ( 7 FDA reports)
CARBOHYDRATE METABOLISM DISORDER ( 7 FDA reports)
CARBON DIOXIDE DECREASED ( 7 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 7 FDA reports)
CHEST WALL ABSCESS ( 7 FDA reports)
CHOREA ( 7 FDA reports)
CLUSTER HEADACHE ( 7 FDA reports)
COELIAC DISEASE ( 7 FDA reports)
COLOSTOMY ( 7 FDA reports)
COLOUR BLINDNESS ( 7 FDA reports)
COMPUTERISED TOMOGRAM CORONARY ARTERY ABNORMAL ( 7 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 7 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 7 FDA reports)
CYSTOCELE ( 7 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 7 FDA reports)
DEATH OF RELATIVE ( 7 FDA reports)
DEPENDENCE ( 7 FDA reports)
DEPRESSION SUICIDAL ( 7 FDA reports)
DEVICE RELATED SEPSIS ( 7 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 7 FDA reports)
DIABETIC COMPLICATION ( 7 FDA reports)
DIABETIC ULCER ( 7 FDA reports)
DIAPHRAGMATIC INJURY ( 7 FDA reports)
DIEULAFOY'S VASCULAR MALFORMATION ( 7 FDA reports)
DRUG ABUSER ( 7 FDA reports)
DRUG INTERACTION INHIBITION ( 7 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 7 FDA reports)
DUODENAL POLYP ( 7 FDA reports)
DYSCALCULIA ( 7 FDA reports)
ENCEPHALITIS ( 7 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 7 FDA reports)
ENERGY INCREASED ( 7 FDA reports)
EPIDURAL ANAESTHESIA ( 7 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 7 FDA reports)
FEELING OF DESPAIR ( 7 FDA reports)
FEMORAL ARTERY OCCLUSION ( 7 FDA reports)
FIBULA FRACTURE ( 7 FDA reports)
FINGER AMPUTATION ( 7 FDA reports)
FINGER DEFORMITY ( 7 FDA reports)
FLUID REPLACEMENT ( 7 FDA reports)
FOOT AMPUTATION ( 7 FDA reports)
FOOT OPERATION ( 7 FDA reports)
FOREIGN BODY ( 7 FDA reports)
FUNGAL SKIN INFECTION ( 7 FDA reports)
GAZE PALSY ( 7 FDA reports)
HAEMATOCRIT ABNORMAL ( 7 FDA reports)
HAEMORRHAGIC INFARCTION ( 7 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 7 FDA reports)
HEMIANOPIA ( 7 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 7 FDA reports)
HEPATITIS TOXIC ( 7 FDA reports)
HERNIA PAIN ( 7 FDA reports)
HODGKIN'S DISEASE ( 7 FDA reports)
HYPERPHAGIA ( 7 FDA reports)
HYPOMETABOLISM ( 7 FDA reports)
IIIRD NERVE PARALYSIS ( 7 FDA reports)
INADEQUATE DIET ( 7 FDA reports)
INCISIONAL HERNIA ( 7 FDA reports)
INFUSION SITE INFECTION ( 7 FDA reports)
INTESTINAL DILATATION ( 7 FDA reports)
INTESTINAL RESECTION ( 7 FDA reports)
INTRACRANIAL HAEMATOMA ( 7 FDA reports)
JAW LESION EXCISION ( 7 FDA reports)
JOINT WARMTH ( 7 FDA reports)
KIDNEY ENLARGEMENT ( 7 FDA reports)
LABILE BLOOD PRESSURE ( 7 FDA reports)
LABYRINTHITIS ( 7 FDA reports)
LARGE INTESTINAL ULCER HAEMORRHAGE ( 7 FDA reports)
LENTIGO ( 7 FDA reports)
LIGAMENT SPRAIN ( 7 FDA reports)
LIP ULCERATION ( 7 FDA reports)
LOCALISED INTRAABDOMINAL FLUID COLLECTION ( 7 FDA reports)
LOCALISED OEDEMA ( 7 FDA reports)
LOGORRHOEA ( 7 FDA reports)
LOSS OF LIBIDO ( 7 FDA reports)
LOW CARDIAC OUTPUT SYNDROME ( 7 FDA reports)
MESENTERIC OCCLUSION ( 7 FDA reports)
METABOLIC ALKALOSIS ( 7 FDA reports)
METASTASES TO PLEURA ( 7 FDA reports)
MONOCYTE COUNT INCREASED ( 7 FDA reports)
MORBID THOUGHTS ( 7 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 7 FDA reports)
MUSCULAR DYSTROPHY ( 7 FDA reports)
NECROTISING FASCIITIS STREPTOCOCCAL ( 7 FDA reports)
NEUROMA ( 7 FDA reports)
OBSTRUCTIVE UROPATHY ( 7 FDA reports)
OESOPHAGEAL MASS ( 7 FDA reports)
OESOPHAGEAL PERFORATION ( 7 FDA reports)
ONYCHOCLASIS ( 7 FDA reports)
ORGANIC ERECTILE DYSFUNCTION ( 7 FDA reports)
OVARIAN MASS ( 7 FDA reports)
PARANEOPLASTIC SYNDROME ( 7 FDA reports)
PENILE PAIN ( 7 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 7 FDA reports)
ABDOMINAL WALL DISORDER ( 6 FDA reports)
ADAMS-STOKES SYNDROME ( 6 FDA reports)
ADRENAL HAEMORRHAGE ( 6 FDA reports)
AMENORRHOEA ( 6 FDA reports)
ANAEMIA MACROCYTIC ( 6 FDA reports)
ANAL CANCER ( 6 FDA reports)
ANAL HAEMORRHAGE ( 6 FDA reports)
ANAPHYLACTOID REACTION ( 6 FDA reports)
ANEURYSM RUPTURED ( 6 FDA reports)
ANGIODYSPLASIA ( 6 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 6 FDA reports)
ANION GAP DECREASED ( 6 FDA reports)
ANISOCYTOSIS ( 6 FDA reports)
ANORECTAL DISCOMFORT ( 6 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 6 FDA reports)
ANTITHROMBIN III DECREASED ( 6 FDA reports)
APPENDICEAL ABSCESS ( 6 FDA reports)
ARTERIAL RUPTURE ( 6 FDA reports)
ATROPHIC VULVOVAGINITIS ( 6 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 6 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 6 FDA reports)
BIOPSY LIVER ABNORMAL ( 6 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 6 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 6 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 6 FDA reports)
BLOOD PRESSURE ORTHOSTATIC ABNORMAL ( 6 FDA reports)
BRACHIAL PLEXOPATHY ( 6 FDA reports)
BULLOUS LUNG DISEASE ( 6 FDA reports)
BUNION ( 6 FDA reports)
CALCULUS URETHRAL ( 6 FDA reports)
CARTILAGE INJURY ( 6 FDA reports)
CATHETERISATION CARDIAC ABNORMAL ( 6 FDA reports)
CELLULITIS ORBITAL ( 6 FDA reports)
CEREBRAL HAEMORRHAGE TRAUMATIC ( 6 FDA reports)
CHONDROPATHY ( 6 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 6 FDA reports)
COLITIS EROSIVE ( 6 FDA reports)
COLONOSCOPY ( 6 FDA reports)
COLORECTAL CANCER METASTATIC ( 6 FDA reports)
CORONARY ANGIOPLASTY ( 6 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 6 FDA reports)
DERMATOMYOSITIS ( 6 FDA reports)
DEVICE DISLOCATION ( 6 FDA reports)
DISLOCATION OF VERTEBRA ( 6 FDA reports)
DISUSE SYNDROME ( 6 FDA reports)
DIVERTICULITIS INTESTINAL HAEMORRHAGIC ( 6 FDA reports)
DIZZINESS EXERTIONAL ( 6 FDA reports)
DRUG LEVEL FLUCTUATING ( 6 FDA reports)
DYSPHORIA ( 6 FDA reports)
DYSPNOEA AT REST ( 6 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ( 6 FDA reports)
ELECTROCARDIOGRAM Q WAVE ABNORMAL ( 6 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 6 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 6 FDA reports)
ENDARTERECTOMY ( 6 FDA reports)
ENDOPHTHALMITIS ( 6 FDA reports)
EPIDIDYMITIS ( 6 FDA reports)
ERYTHEMA NODOSUM ( 6 FDA reports)
ERYTHROPOIESIS ABNORMAL ( 6 FDA reports)
EUPHORIC MOOD ( 6 FDA reports)
EXANTHEM ( 6 FDA reports)
EXCESSIVE EYE BLINKING ( 6 FDA reports)
EYE PRURITUS ( 6 FDA reports)
EYELID DISORDER ( 6 FDA reports)
FEMORAL NERVE PALSY ( 6 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 6 FDA reports)
GASTROINTESTINAL TOXICITY ( 6 FDA reports)
GIARDIASIS ( 6 FDA reports)
GLIOSIS ( 6 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 6 FDA reports)
GLOSSOPTOSIS ( 6 FDA reports)
GROIN ABSCESS ( 6 FDA reports)
HAEMOPHILUS BACTERAEMIA ( 6 FDA reports)
HEAD AND NECK CANCER ( 6 FDA reports)
HEART VALVE STENOSIS ( 6 FDA reports)
HEPATIC NEOPLASM ( 6 FDA reports)
HIP DEFORMITY ( 6 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 6 FDA reports)
HOMOCYSTINAEMIA ( 6 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 6 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 6 FDA reports)
HYPOPROTHROMBINAEMIA ( 6 FDA reports)
ILIAC ARTERY EMBOLISM ( 6 FDA reports)
IMPLANT SITE INFECTION ( 6 FDA reports)
INFECTED CYST ( 6 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 6 FDA reports)
INFUSION SITE PAIN ( 6 FDA reports)
INJECTION SITE NECROSIS ( 6 FDA reports)
INJECTION SITE WARMTH ( 6 FDA reports)
INTENTIONAL MISUSE ( 6 FDA reports)
INTERNAL FIXATION OF FRACTURE ( 6 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 6 FDA reports)
INTUBATION ( 6 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 6 FDA reports)
LACTOSE INTOLERANCE ( 6 FDA reports)
LARYNGOSPASM ( 6 FDA reports)
LIP BLISTER ( 6 FDA reports)
LITHOTRIPSY ( 6 FDA reports)
LOWER EXTREMITY MASS ( 6 FDA reports)
LUMBOSACRAL PLEXUS LESION ( 6 FDA reports)
LUNG TRANSPLANT ( 6 FDA reports)
LYMPHOCYTIC INFILTRATION ( 6 FDA reports)
LYMPHORRHOEA ( 6 FDA reports)
MASTITIS ( 6 FDA reports)
MAXILLOFACIAL OPERATION ( 6 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 6 FDA reports)
MENISCAL DEGENERATION ( 6 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 6 FDA reports)
METASTASES TO PERITONEUM ( 6 FDA reports)
METASTASES TO SKIN ( 6 FDA reports)
MICROCOCCUS INFECTION ( 6 FDA reports)
MOUTH INJURY ( 6 FDA reports)
NAIL DISORDER ( 6 FDA reports)
NARCOLEPSY ( 6 FDA reports)
NASAL DRYNESS ( 6 FDA reports)
NEOPLASM SKIN ( 6 FDA reports)
NEPHROGENIC ANAEMIA ( 6 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 6 FDA reports)
NEPHROGENIC FIBROSING DERMOPATHY ( 6 FDA reports)
OESOPHAGEAL DILATATION ( 6 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 6 FDA reports)
OLIGOHYDRAMNIOS ( 6 FDA reports)
OPEN ANGLE GLAUCOMA ( 6 FDA reports)
OPTIC NEURITIS ( 6 FDA reports)
ORAL FUNGAL INFECTION ( 6 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 6 FDA reports)
ORGANISING PNEUMONIA ( 6 FDA reports)
PANCREATIC NEOPLASM ( 6 FDA reports)
PARTIAL SEIZURES ( 6 FDA reports)
PELVIC VENOUS THROMBOSIS ( 6 FDA reports)
PENILE HAEMORRHAGE ( 6 FDA reports)
PERIORBITAL HAEMORRHAGE ( 6 FDA reports)
PERIRECTAL ABSCESS ( 6 FDA reports)
PERITONEAL DISORDER ( 6 FDA reports)
PHRENIC NERVE PARALYSIS ( 6 FDA reports)
PHYSICAL ASSAULT ( 6 FDA reports)
POLYCHROMASIA ( 6 FDA reports)
PORENCEPHALY ( 6 FDA reports)
PSEUDOCYST ( 6 FDA reports)
PYODERMA GANGRENOSUM ( 6 FDA reports)
RADICULAR PAIN ( 6 FDA reports)
RAYNAUD'S PHENOMENON ( 6 FDA reports)
RETINAL DEGENERATION ( 6 FDA reports)
RETINAL TEAR ( 6 FDA reports)
SALIVA ALTERED ( 6 FDA reports)
SENSATION OF PRESSURE ( 6 FDA reports)
SEPTIC EMBOLUS ( 6 FDA reports)
SLUGGISHNESS ( 6 FDA reports)
SPIDER VEIN ( 6 FDA reports)
SPLENECTOMY ( 6 FDA reports)
SPONDYLITIS ( 6 FDA reports)
SPUTUM PURULENT ( 6 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 6 FDA reports)
STARING ( 6 FDA reports)
STILLBIRTH ( 6 FDA reports)
SUPERINFECTION ( 6 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 6 FDA reports)
SUTURE INSERTION ( 6 FDA reports)
SUTURE RUPTURE ( 6 FDA reports)
THERAPY REGIMEN CHANGED ( 6 FDA reports)
THORACOTOMY ( 6 FDA reports)
THROMBOTIC STROKE ( 6 FDA reports)
THYROID HORMONE REPLACEMENT THERAPY ( 6 FDA reports)
TOBACCO USER ( 6 FDA reports)
TONGUE NEOPLASM ( 6 FDA reports)
TOOTH AVULSION ( 6 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 6 FDA reports)
URETERAL STENT INSERTION ( 6 FDA reports)
URETHRAL OBSTRUCTION ( 6 FDA reports)
VAGINITIS BACTERIAL ( 6 FDA reports)
VASCULAR OCCLUSION ( 6 FDA reports)
VENOUS HAEMORRHAGE ( 6 FDA reports)
VESTIBULAR DISORDER ( 6 FDA reports)
YAWNING ( 6 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 5 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 5 FDA reports)
PERSECUTORY DELUSION ( 5 FDA reports)
PHIMOSIS ( 5 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 5 FDA reports)
PLANTAR ERYTHEMA ( 5 FDA reports)
PLATELET DISORDER ( 5 FDA reports)
PLEURAL HAEMORRHAGE ( 5 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 5 FDA reports)
PNEUMONIA ESCHERICHIA ( 5 FDA reports)
PNEUMONIA LEGIONELLA ( 5 FDA reports)
PNEUMOPERITONEUM ( 5 FDA reports)
POIKILOCYTOSIS ( 5 FDA reports)
POST PROCEDURAL DISCHARGE ( 5 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 5 FDA reports)
POSTOPERATIVE ILEUS ( 5 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 5 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 5 FDA reports)
PROSTATIC HAEMORRHAGE ( 5 FDA reports)
PROTEIN C DEFICIENCY ( 5 FDA reports)
PROTRUSION TONGUE ( 5 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 5 FDA reports)
PSYCHIATRIC DECOMPENSATION ( 5 FDA reports)
PSYCHOSOMATIC DISEASE ( 5 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 5 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 5 FDA reports)
RADIATION MUCOSITIS ( 5 FDA reports)
RASH MORBILLIFORM ( 5 FDA reports)
RECTAL DISCHARGE ( 5 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 5 FDA reports)
RENAL NEOPLASM ( 5 FDA reports)
SACRALISATION ( 5 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 5 FDA reports)
SALIVARY HYPERSECRETION ( 5 FDA reports)
SCIATIC NERVE INJURY ( 5 FDA reports)
SCLERAL DISCOLOURATION ( 5 FDA reports)
SCROTAL SWELLING ( 5 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 5 FDA reports)
SERUM FERRITIN DECREASED ( 5 FDA reports)
SHIFT TO THE LEFT ( 5 FDA reports)
SHOULDER PAIN ( 5 FDA reports)
SIALOADENITIS ( 5 FDA reports)
SKIN CANCER METASTATIC ( 5 FDA reports)
SKIN CHAPPED ( 5 FDA reports)
SKIN FRAGILITY ( 5 FDA reports)
SKIN INFLAMMATION ( 5 FDA reports)
SKIN SWELLING ( 5 FDA reports)
SKIN WRINKLING ( 5 FDA reports)
SKULL FRACTURE ( 5 FDA reports)
SLEEP WALKING ( 5 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 5 FDA reports)
SOFT TISSUE HAEMORRHAGE ( 5 FDA reports)
SOFT TISSUE INJURY ( 5 FDA reports)
SPLEEN DISORDER ( 5 FDA reports)
SPONTANEOUS HAEMATOMA ( 5 FDA reports)
SPUTUM ABNORMAL ( 5 FDA reports)
SUBMANDIBULAR MASS ( 5 FDA reports)
SUBRETINAL FIBROSIS ( 5 FDA reports)
SUPRAPUBIC PAIN ( 5 FDA reports)
TACHYARRHYTHMIA ( 5 FDA reports)
TESTICULAR SWELLING ( 5 FDA reports)
THERAPY CESSATION ( 5 FDA reports)
THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 5 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 5 FDA reports)
THYROXINE FREE INCREASED ( 5 FDA reports)
TOOTH INJURY ( 5 FDA reports)
TRANSFUSION REACTION ( 5 FDA reports)
TRAUMATIC BRAIN INJURY ( 5 FDA reports)
TRAUMATIC HAEMORRHAGE ( 5 FDA reports)
TRAUMATIC SHOCK ( 5 FDA reports)
UNRESPONSIVE TO PAIN STIMULI ( 5 FDA reports)
URINARY HESITATION ( 5 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 5 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 5 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 5 FDA reports)
UTERINE MALPOSITION ( 5 FDA reports)
VARICELLA ( 5 FDA reports)
VENTRICULAR DYSKINESIA ( 5 FDA reports)
VENTRICULAR FLUTTER ( 5 FDA reports)
VITREOUS OPACITIES ( 5 FDA reports)
VOLUME BLOOD INCREASED ( 5 FDA reports)
XEROSIS ( 5 FDA reports)
YELLOW SKIN ( 5 FDA reports)
ABDOMINAL STRANGULATED HERNIA ( 5 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 5 FDA reports)
ABNORMAL CLOTTING FACTOR ( 5 FDA reports)
ACCELERATED HYPERTENSION ( 5 FDA reports)
ACCIDENTAL DEATH ( 5 FDA reports)
ANAEMIA POSTOPERATIVE ( 5 FDA reports)
ANAESTHETIC COMPLICATION ( 5 FDA reports)
ANAL DISCOMFORT ( 5 FDA reports)
ANOGENITAL WARTS ( 5 FDA reports)
ANTI-INSULIN ANTIBODY ( 5 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 5 FDA reports)
APPARENT DEATH ( 5 FDA reports)
APPENDICITIS PERFORATED ( 5 FDA reports)
APPLICATION SITE DERMATITIS ( 5 FDA reports)
APPLICATION SITE RASH ( 5 FDA reports)
ARTERIOSPASM CORONARY ( 5 FDA reports)
ARTERIOVENOUS FISTULA OPERATION ( 5 FDA reports)
ARTHROSCOPY ( 5 FDA reports)
ATRIAL HYPERTROPHY ( 5 FDA reports)
AVULSION FRACTURE ( 5 FDA reports)
BENIGN COLONIC NEOPLASM ( 5 FDA reports)
BLADDER DYSFUNCTION ( 5 FDA reports)
BLADDER PROLAPSE ( 5 FDA reports)
BLADDER SPASM ( 5 FDA reports)
BLOOD CORTISOL INCREASED ( 5 FDA reports)
BONE ATROPHY ( 5 FDA reports)
BONE CYST ( 5 FDA reports)
BONE DEVELOPMENT ABNORMAL ( 5 FDA reports)
BONE FRAGMENTATION ( 5 FDA reports)
BREAST NECROSIS ( 5 FDA reports)
CARCINOMA IN SITU OF EYE ( 5 FDA reports)
CARDIAC PACEMAKER MALFUNCTION ( 5 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 5 FDA reports)
CAROTID ENDARTERECTOMY ( 5 FDA reports)
CATHETER SITE DISCHARGE ( 5 FDA reports)
CATHETER SITE ERYTHEMA ( 5 FDA reports)
CATHETER THROMBOSIS ( 5 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 5 FDA reports)
CEREBELLAR ATAXIA ( 5 FDA reports)
CERVICITIS ( 5 FDA reports)
CHAPPED LIPS ( 5 FDA reports)
CHEYNE-STOKES RESPIRATION ( 5 FDA reports)
CLONIC CONVULSION ( 5 FDA reports)
CLUBBING ( 5 FDA reports)
CLUMSINESS ( 5 FDA reports)
COLECTOMY ( 5 FDA reports)
CONJUNCTIVAL PALLOR ( 5 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 5 FDA reports)
CONUS MEDULLARIS SYNDROME ( 5 FDA reports)
CORNEAL DYSTROPHY ( 5 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 5 FDA reports)
CRANIAL NERVE PALSIES MULTIPLE ( 5 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 5 FDA reports)
CUTANEOUS SARCOIDOSIS ( 5 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 5 FDA reports)
DERMATITIS ATOPIC ( 5 FDA reports)
DEVICE DAMAGE ( 5 FDA reports)
DIABETIC COMA ( 5 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 5 FDA reports)
DISSEMINATED TUBERCULOSIS ( 5 FDA reports)
DRUG CLEARANCE DECREASED ( 5 FDA reports)
DYSMORPHISM ( 5 FDA reports)
EOSINOPHIL COUNT DECREASED ( 5 FDA reports)
EXTERNAL EAR DISORDER ( 5 FDA reports)
EYE EXCISION ( 5 FDA reports)
EYELID MARGIN CRUSTING ( 5 FDA reports)
FACE AND MOUTH X-RAY ABNORMAL ( 5 FDA reports)
FACTOR V LEIDEN MUTATION ( 5 FDA reports)
FEELING GUILTY ( 5 FDA reports)
FLAT ANTERIOR CHAMBER OF EYE ( 5 FDA reports)
FOREIGN BODY ASPIRATION ( 5 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 5 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 5 FDA reports)
FUNGAL SEPSIS ( 5 FDA reports)
GALLOP RHYTHM PRESENT ( 5 FDA reports)
GASTRIC DILATATION ( 5 FDA reports)
GASTRIC VARICES ( 5 FDA reports)
GASTRODUODENAL ULCER ( 5 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA ( 5 FDA reports)
GASTROINTESTINAL NEOPLASM ( 5 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 5 FDA reports)
GASTROINTESTINAL ULCER PERFORATION ( 5 FDA reports)
GINGIVAL BLISTER ( 5 FDA reports)
GINGIVAL OEDEMA ( 5 FDA reports)
GLIOBLASTOMA ( 5 FDA reports)
GLYCOSURIA ( 5 FDA reports)
GRIMACING ( 5 FDA reports)
HAEMANGIOMA OF LIVER ( 5 FDA reports)
HAEMOGLOBINURIA ( 5 FDA reports)
HAEMOPHILUS INFECTION ( 5 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 5 FDA reports)
HELICOBACTER GASTRITIS ( 5 FDA reports)
HEPATIC CALCIFICATION ( 5 FDA reports)
HEPATIC PAIN ( 5 FDA reports)
HEPATORENAL FAILURE ( 5 FDA reports)
HYPERCHLORHYDRIA ( 5 FDA reports)
HYPERGLYCAEMIC HYPEROSMOLAR NONKETOTIC SYNDROME ( 5 FDA reports)
HYPERPLASTIC CHOLECYSTOPATHY ( 5 FDA reports)
HYPERVOLAEMIA ( 5 FDA reports)
HYPNOPOMPIC HALLUCINATION ( 5 FDA reports)
HYPOGEUSIA ( 5 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 5 FDA reports)
ILEITIS ( 5 FDA reports)
IMPATIENCE ( 5 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 5 FDA reports)
INDURATION ( 5 FDA reports)
INFUSION SITE HAEMORRHAGE ( 5 FDA reports)
INJECTION SITE BURNING ( 5 FDA reports)
INJECTION SITE INFLAMMATION ( 5 FDA reports)
INJECTION SITE URTICARIA ( 5 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 5 FDA reports)
INTERCOSTAL NEURALGIA ( 5 FDA reports)
INTESTINAL FISTULA ( 5 FDA reports)
INTESTINAL MASS ( 5 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 5 FDA reports)
INTRAMEDULLARY ROD INSERTION ( 5 FDA reports)
KIDNEY FIBROSIS ( 5 FDA reports)
LIPID METABOLISM DISORDER ( 5 FDA reports)
LIPIDS INCREASED ( 5 FDA reports)
LOOSE STOOLS ( 5 FDA reports)
LOSS OF PROPRIOCEPTION ( 5 FDA reports)
LOW BIRTH WEIGHT BABY ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
LYMPH NODE PAIN ( 5 FDA reports)
LYMPHATIC SYSTEM NEOPLASM ( 5 FDA reports)
LYMPHOCELE ( 5 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 5 FDA reports)
MADAROSIS ( 5 FDA reports)
MEAN CELL HAEMOGLOBIN DECREASED ( 5 FDA reports)
MEDIASTINAL DISORDER ( 5 FDA reports)
MELANOCYTIC NAEVUS ( 5 FDA reports)
MENINGOENCEPHALITIS BACTERIAL ( 5 FDA reports)
MENOPAUSE ( 5 FDA reports)
MESENTERIC ARTERY EMBOLISM ( 5 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 5 FDA reports)
METASTASES TO MUSCLE ( 5 FDA reports)
METATARSUS PRIMUS VARUS ( 5 FDA reports)
MICROALBUMINURIA ( 5 FDA reports)
MICTURITION DISORDER ( 5 FDA reports)
MIXED HYPERLIPIDAEMIA ( 5 FDA reports)
MONONEUROPATHY MULTIPLEX ( 5 FDA reports)
MONOPARESIS ( 5 FDA reports)
MUSCLE CRAMP ( 5 FDA reports)
MUSCLE NECROSIS ( 5 FDA reports)
NECROSIS ISCHAEMIC ( 5 FDA reports)
NEUROPATHIC PAIN ( 5 FDA reports)
NON-HODGKIN'S LYMPHOMA RECURRENT ( 5 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 5 FDA reports)
OCULAR DISCOMFORT ( 5 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 5 FDA reports)
ONYCHOLYSIS ( 5 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 5 FDA reports)
OSTEOPOROTIC FRACTURE ( 5 FDA reports)
OXYGEN SATURATION ABNORMAL ( 5 FDA reports)
PACEMAKER COMPLICATION ( 5 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 5 FDA reports)
PANCREATIC NECROSIS ( 5 FDA reports)
PEPTIC ULCER HAEMORRHAGE ( 5 FDA reports)
5-HYDROXYINDOLACETIC ACID INCREASED ( 4 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 4 FDA reports)
ABORTION MISSED ( 4 FDA reports)
ABSCESS INTESTINAL ( 4 FDA reports)
ACARODERMATITIS ( 4 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 4 FDA reports)
ACCOMMODATION DISORDER ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 4 FDA reports)
ACUTE LEUKAEMIA ( 4 FDA reports)
ACUTE PSYCHOSIS ( 4 FDA reports)
ADENOCARCINOMA PANCREAS ( 4 FDA reports)
ADRENAL CORTEX NECROSIS ( 4 FDA reports)
ADRENAL NEOPLASM ( 4 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 4 FDA reports)
ALBUMIN GLOBULIN RATIO DECREASED ( 4 FDA reports)
ANAL SPHINCTER ATONY ( 4 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 4 FDA reports)
ANGIOGRAM ( 4 FDA reports)
ANGIOMYOLIPOMA ( 4 FDA reports)
ANKYLOSING SPONDYLITIS ( 4 FDA reports)
AORTIC ATHEROSCLEROSIS ( 4 FDA reports)
AORTIC DISSECTION RUPTURE ( 4 FDA reports)
AORTIC VALVE REPAIR ( 4 FDA reports)
APGAR SCORE LOW ( 4 FDA reports)
ARTERITIS ( 4 FDA reports)
ARTIFICIAL CROWN PROCEDURE ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 4 FDA reports)
AURA ( 4 FDA reports)
AURICULAR SWELLING ( 4 FDA reports)
BACTERIA URINE IDENTIFIED ( 4 FDA reports)
BASAL GANGLIA INFARCTION ( 4 FDA reports)
BASOPHIL COUNT INCREASED ( 4 FDA reports)
BELLIGERENCE ( 4 FDA reports)
BIFASCICULAR BLOCK ( 4 FDA reports)
BILIARY SEPSIS ( 4 FDA reports)
BLADDER DILATATION ( 4 FDA reports)
BLADDER OBSTRUCTION ( 4 FDA reports)
BLAST CELL COUNT INCREASED ( 4 FDA reports)
BLOOD CALCIUM ABNORMAL ( 4 FDA reports)
BLOOD CORTISOL DECREASED ( 4 FDA reports)
BLOOD CREATINE ABNORMAL ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 4 FDA reports)
BLOOD GASES ABNORMAL ( 4 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 4 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 4 FDA reports)
BLUNTED AFFECT ( 4 FDA reports)
BRAIN COMPRESSION ( 4 FDA reports)
BRAIN DAMAGE ( 4 FDA reports)
BRAIN STEM SYNDROME ( 4 FDA reports)
BRAIN TUMOUR OPERATION ( 4 FDA reports)
BREAKTHROUGH PAIN ( 4 FDA reports)
BREAST CANCER MALE ( 4 FDA reports)
BRONCHITIS ACUTE ( 4 FDA reports)
BRONCHITIS MORAXELLA ( 4 FDA reports)
BUTTOCK PAIN ( 4 FDA reports)
CALCIFICATION METASTATIC ( 4 FDA reports)
CARBON DIOXIDE ABNORMAL ( 4 FDA reports)
CARDIAC FAILURE HIGH OUTPUT ( 4 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 4 FDA reports)
CARDIAC PACEMAKER REPLACEMENT ( 4 FDA reports)
CARDIAC SEPTAL DEFECT ( 4 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 4 FDA reports)
CAUDA EQUINA SYNDROME ( 4 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 4 FDA reports)
CELL MARKER INCREASED ( 4 FDA reports)
CELLULITIS GANGRENOUS ( 4 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 4 FDA reports)
CEREBELLAR ATROPHY ( 4 FDA reports)
CEREBRAL CALCIFICATION ( 4 FDA reports)
CHEST WALL PAIN ( 4 FDA reports)
CHONDRODYSTROPHY ( 4 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 4 FDA reports)
CLONUS ( 4 FDA reports)
CLOSED HEAD INJURY ( 4 FDA reports)
COAGULATION FACTOR XIII LEVEL DECREASED ( 4 FDA reports)
COLLATERAL CIRCULATION ( 4 FDA reports)
COLONIC FISTULA ( 4 FDA reports)
COMMINUTED FRACTURE ( 4 FDA reports)
COMPLICATION OF DEVICE INSERTION ( 4 FDA reports)
CONGENITAL NOSE MALFORMATION ( 4 FDA reports)
CONJUNCTIVAL DISORDER ( 4 FDA reports)
CONNECTIVE TISSUE INFLAMMATION ( 4 FDA reports)
CONTRAST MEDIA ALLERGY ( 4 FDA reports)
CRANIECTOMY ( 4 FDA reports)
CSF PROTEIN INCREASED ( 4 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 4 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 4 FDA reports)
DACRYOCYSTORHINOSTOMY ( 4 FDA reports)
DANDRUFF ( 4 FDA reports)
DELIRIUM FEBRILE ( 4 FDA reports)
DELUSION OF REPLACEMENT ( 4 FDA reports)
DENGUE FEVER ( 4 FDA reports)
DENTAL DISCOMFORT ( 4 FDA reports)
DENTAL TREATMENT ( 4 FDA reports)
DIAPHRAGMATIC HERNIA ( 4 FDA reports)
DNA ANTIBODY POSITIVE ( 4 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 4 FDA reports)
DRUG THERAPY ( 4 FDA reports)
DUODENAL PERFORATION ( 4 FDA reports)
DUODENITIS HAEMORRHAGIC ( 4 FDA reports)
ENDOTHELIAL DYSFUNCTION ( 4 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 4 FDA reports)
EOSINOPHILIC OESOPHAGITIS ( 4 FDA reports)
ESCHAR ( 4 FDA reports)
EXERCISE TEST ABNORMAL ( 4 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 4 FDA reports)
FACIAL NERVE DISORDER ( 4 FDA reports)
FEAR OF DEATH ( 4 FDA reports)
FEAR OF FALLING ( 4 FDA reports)
FEMORAL PULSE DECREASED ( 4 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 4 FDA reports)
FIBRIN INCREASED ( 4 FDA reports)
FLUID IMBALANCE ( 4 FDA reports)
FOREIGN BODY TRAUMA ( 4 FDA reports)
GALLBLADDER OPERATION ( 4 FDA reports)
GALLBLADDER PERFORATION ( 4 FDA reports)
GASTRIC BYPASS ( 4 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 4 FDA reports)
GENITAL HAEMORRHAGE ( 4 FDA reports)
GILBERT'S SYNDROME ( 4 FDA reports)
GINGIVAL HYPERTROPHY ( 4 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 4 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 4 FDA reports)
HAEMOCONCENTRATION ( 4 FDA reports)
HAIR TEXTURE ABNORMAL ( 4 FDA reports)
HEMIANOPIA HOMONYMOUS ( 4 FDA reports)
HEPATIC ISCHAEMIA ( 4 FDA reports)
HEPATIC RUPTURE ( 4 FDA reports)
HEPATITIS VIRAL ( 4 FDA reports)
HIDRADENITIS ( 4 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 4 FDA reports)
HIGH RISK PREGNANCY ( 4 FDA reports)
HISTOPLASMOSIS ( 4 FDA reports)
HOARSENESS ( 4 FDA reports)
HOSPICE CARE ( 4 FDA reports)
HYPERAMYLASAEMIA ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPERINSULINAEMIA ( 4 FDA reports)
HYPERMETROPIA ( 4 FDA reports)
HYPERPYREXIA ( 4 FDA reports)
HYPERTROPHY ( 4 FDA reports)
HYPOCHONDRIASIS ( 4 FDA reports)
IMPLANT SITE HAEMATOMA ( 4 FDA reports)
IMPLANTABLE DEFIBRILLATOR REPLACEMENT ( 4 FDA reports)
INAPPROPRIATE AFFECT ( 4 FDA reports)
INCISION SITE INFECTION ( 4 FDA reports)
INCORRECT STORAGE OF DRUG ( 4 FDA reports)
INFECTION PARASITIC ( 4 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 4 FDA reports)
INTESTINAL OPERATION ( 4 FDA reports)
INTRA-ABDOMINAL PRESSURE INCREASED ( 4 FDA reports)
IRIS CYST ( 4 FDA reports)
IRITIS ( 4 FDA reports)
JOINT CREPITATION ( 4 FDA reports)
KIDNEY RUPTURE ( 4 FDA reports)
LACRIMAL DUCT PROCEDURE ( 4 FDA reports)
LARGE INTESTINAL STRICTURE ( 4 FDA reports)
LARYNGOPHARYNGITIS ( 4 FDA reports)
LICHEN PLANUS ( 4 FDA reports)
LIVE BIRTH ( 4 FDA reports)
LIVER TRANSPLANT REJECTION ( 4 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 4 FDA reports)
LUNG ABSCESS ( 4 FDA reports)
LYMPHADENECTOMY ( 4 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 4 FDA reports)
LYMPHOCYTOSIS ( 4 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 4 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 4 FDA reports)
MEAN CELL VOLUME DECREASED ( 4 FDA reports)
MENINGEAL NEOPLASM ( 4 FDA reports)
MENINGITIS ASEPTIC ( 4 FDA reports)
METASTATIC LYMPHOMA ( 4 FDA reports)
MUSCLE FIBROSIS ( 4 FDA reports)
MYCOPLASMA INFECTION ( 4 FDA reports)
MYCOSIS FUNGOIDES ( 4 FDA reports)
MYELOID LEUKAEMIA ( 4 FDA reports)
MYOGLOBINURIA ( 4 FDA reports)
MYXOEDEMA ( 4 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
NECK MASS ( 4 FDA reports)
NEOPLASM PROSTATE ( 4 FDA reports)
NEPHRECTOMY ( 4 FDA reports)
NEUTROPHIL TOXIC GRANULATION PRESENT ( 4 FDA reports)
NIGHT BLINDNESS ( 4 FDA reports)
NODULE ON EXTREMITY ( 4 FDA reports)
NON-NEUTRALISING ANTIBODIES POSITIVE ( 4 FDA reports)
ONYCHOMADESIS ( 4 FDA reports)
OOPHORECTOMY ( 4 FDA reports)
ORAL MUCOSAL BLISTERING ( 4 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 4 FDA reports)
OROPHARYNGEAL SWELLING ( 4 FDA reports)
ORTHOSTATIC INTOLERANCE ( 4 FDA reports)
OSTECTOMY ( 4 FDA reports)
OTOTOXICITY ( 4 FDA reports)
OVARIAN CANCER METASTATIC ( 4 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 4 FDA reports)
OXYGEN SATURATION ( 4 FDA reports)
PAIN EXACERBATED ( 4 FDA reports)
PALATAL DISORDER ( 4 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 4 FDA reports)
PARALYSIS FLACCID ( 4 FDA reports)
PATELLA FRACTURE ( 4 FDA reports)
PENILE NECROSIS ( 4 FDA reports)
PERITONEAL HAEMATOMA ( 4 FDA reports)
PERITONSILLITIS ( 4 FDA reports)
PERSONALITY DISORDER ( 4 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 4 FDA reports)
PHLEBOTHROMBOSIS ( 4 FDA reports)
PLASMA VISCOSITY DECREASED ( 4 FDA reports)
PLATELET COUNT ABNORMAL ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PNEUMOMEDIASTINUM ( 4 FDA reports)
PNEUMONIA HAEMOPHILUS ( 4 FDA reports)
PO2 INCREASED ( 4 FDA reports)
PORIOMANIA ( 4 FDA reports)
POSTICTAL PARALYSIS ( 4 FDA reports)
POSTOPERATIVE THROMBOSIS ( 4 FDA reports)
POSTURING ( 4 FDA reports)
PREGNANCY WITH CONTRACEPTIVE DEVICE ( 4 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 4 FDA reports)
PRESCRIBED OVERDOSE ( 4 FDA reports)
PRINZMETAL ANGINA ( 4 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 4 FDA reports)
PROSTATE CANCER RECURRENT ( 4 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 4 FDA reports)
PSEUDOPOLYPOSIS ( 4 FDA reports)
PUBIS FRACTURE ( 4 FDA reports)
PULMONARY SARCOIDOSIS ( 4 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 4 FDA reports)
PUNCTURE SITE INFECTION ( 4 FDA reports)
PUPILLARY DISORDER ( 4 FDA reports)
PURPURA SENILE ( 4 FDA reports)
PYELOCALIECTASIS ( 4 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 4 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 4 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE DECREASED ( 4 FDA reports)
REHABILITATION THERAPY ( 4 FDA reports)
RENAL ARTERY ARTERIOSCLEROSIS ( 4 FDA reports)
RENAL TUBULAR ATROPHY ( 4 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 4 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 4 FDA reports)
RETROPERITONEAL CANCER ( 4 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 4 FDA reports)
RHYTHM IDIOVENTRICULAR ( 4 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
ROTATOR CUFF REPAIR ( 4 FDA reports)
SARCOMA ( 4 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 4 FDA reports)
SCOTOMA ( 4 FDA reports)
SCROTAL HAEMATOMA ( 4 FDA reports)
SEBORRHOEA ( 4 FDA reports)
SHOULDER OPERATION ( 4 FDA reports)
SIGMOIDITIS ( 4 FDA reports)
SIMPLE PARTIAL SEIZURES ( 4 FDA reports)
SINUSITIS BACTERIAL ( 4 FDA reports)
SKIN GRAFT FAILURE ( 4 FDA reports)
SKIN LESION EXCISION ( 4 FDA reports)
SKIN MASS ( 4 FDA reports)
SKIN ODOUR ABNORMAL ( 4 FDA reports)
SPLENIC HAEMATOMA ( 4 FDA reports)
SPLENIC MARGINAL ZONE LYMPHOMA ( 4 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 4 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 4 FDA reports)
STENOTROPHOMONAS SEPSIS ( 4 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 4 FDA reports)
SUDDEN HEARING LOSS ( 4 FDA reports)
SUPERIOR VENA CAVAL STENOSIS ( 4 FDA reports)
SYSTOLIC HYPERTENSION ( 4 FDA reports)
TALIPES ( 4 FDA reports)
TEETH BRITTLE ( 4 FDA reports)
TEMPERATURE DIFFERENCE OF EXTREMITIES ( 4 FDA reports)
THERAPEUTIC PROCEDURE ( 4 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 4 FDA reports)
THORACIC HAEMORRHAGE ( 4 FDA reports)
THROAT CANCER ( 4 FDA reports)
THROMBOEMBOLIC STROKE ( 4 FDA reports)
THYROID MASS ( 4 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 4 FDA reports)
TONGUE PARALYSIS ( 4 FDA reports)
TONSILLITIS ( 4 FDA reports)
TORULOPSIS INFECTION ( 4 FDA reports)
TRACHEAL DISORDER ( 4 FDA reports)
TRACHEAL HAEMORRHAGE ( 4 FDA reports)
TRACHEAL OPERATION ( 4 FDA reports)
TRACHEOBRONCHITIS ( 4 FDA reports)
TRIGGER FINGER ( 4 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 4 FDA reports)
ULNA FRACTURE ( 4 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 4 FDA reports)
UPPER EXTREMITY MASS ( 4 FDA reports)
URETERIC DILATATION ( 4 FDA reports)
URINARY SEDIMENT ABNORMAL ( 4 FDA reports)
URINE KETONE BODY PRESENT ( 4 FDA reports)
URINE ODOUR ABNORMAL ( 4 FDA reports)
URTICARIA GENERALISED ( 4 FDA reports)
UTERINE HAEMORRHAGE ( 4 FDA reports)
VASCULAR INJURY ( 4 FDA reports)
VASCULAR RESISTANCE PULMONARY INCREASED ( 4 FDA reports)
VENOUS PRESSURE INCREASED ( 4 FDA reports)
VENOUS RECANALISATION ( 4 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 4 FDA reports)
VIRAL PERICARDITIS ( 4 FDA reports)
VITAMIN K DECREASED ( 4 FDA reports)
WALKING DISABILITY ( 4 FDA reports)
WEIGHT ABNORMAL ( 4 FDA reports)
WOUND ABSCESS ( 4 FDA reports)
WOUND INFECTION BACTERIAL ( 4 FDA reports)
WOUND INFECTION PSEUDOMONAS ( 4 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 3 FDA reports)
PHANTOM PAIN ( 3 FDA reports)
PITUITARY TUMOUR BENIGN ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
POLYCYSTIC OVARIES ( 3 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 3 FDA reports)
POROKERATOSIS ( 3 FDA reports)
POST PROCEDURAL DIARRHOEA ( 3 FDA reports)
POSTICTAL STATE ( 3 FDA reports)
PRE-ECLAMPSIA ( 3 FDA reports)
PREMATURE DELIVERY ( 3 FDA reports)
PRODUCT ADHESION ISSUE ( 3 FDA reports)
PRODUCT COMMINGLING ( 3 FDA reports)
PROSTATIC INTRAEPITHELIAL NEOPLASIA ( 3 FDA reports)
PROTEIN S DECREASED ( 3 FDA reports)
PROTHROMBIN TIME RATIO ABNORMAL ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 3 FDA reports)
PSEUDOPOLYP ( 3 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 3 FDA reports)
PULMONARY FUNCTION TEST ( 3 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 3 FDA reports)
PULMONARY VEIN OCCLUSION ( 3 FDA reports)
QUADRUPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
RADIAL PULSE ABNORMAL ( 3 FDA reports)
RECTAL ADENOMA ( 3 FDA reports)
RECTAL PROLAPSE ( 3 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 3 FDA reports)
REFRACTORY ANAEMIA ( 3 FDA reports)
RENAL ARTERIOSCLEROSIS ( 3 FDA reports)
RENAL ARTERY THROMBOSIS ( 3 FDA reports)
RESORPTION BONE INCREASED ( 3 FDA reports)
RETINITIS PIGMENTOSA ( 3 FDA reports)
RHEUMATOID FACTOR INCREASED ( 3 FDA reports)
RHINALGIA ( 3 FDA reports)
RIB DEFORMITY ( 3 FDA reports)
ROUTINE HEALTH MAINTENANCE ( 3 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 3 FDA reports)
SCAN ABDOMEN ABNORMAL ( 3 FDA reports)
SCLEREMA ( 3 FDA reports)
SCLERITIS ( 3 FDA reports)
SCLEROSING ENCAPSULATING PERITONITIS ( 3 FDA reports)
SELF ESTEEM DECREASED ( 3 FDA reports)
SELF-INJURIOUS IDEATION ( 3 FDA reports)
SENILE OSTEOPOROSIS ( 3 FDA reports)
SINUS RHYTHM ( 3 FDA reports)
SKIN BLEEDING ( 3 FDA reports)
SKIN DESQUAMATION ( 3 FDA reports)
SKIN DISCOMFORT ( 3 FDA reports)
SKIN HYPOPIGMENTATION ( 3 FDA reports)
SKIN INJURY ( 3 FDA reports)
SKIN NODULE ( 3 FDA reports)
SKIN STRIAE ( 3 FDA reports)
SKIN ULCER HAEMORRHAGE ( 3 FDA reports)
SMALL CELL CARCINOMA ( 3 FDA reports)
SMALL INTESTINAL PERFORATION ( 3 FDA reports)
SMOKER ( 3 FDA reports)
SPINAL CORD INFARCTION ( 3 FDA reports)
SPINAL CORD OPERATION ( 3 FDA reports)
SPLENIC HAEMORRHAGE ( 3 FDA reports)
SPLINTER HAEMORRHAGES ( 3 FDA reports)
SPUTUM RETENTION ( 3 FDA reports)
STATUS MIGRAINOSUS ( 3 FDA reports)
STENOTROPHOMONAS TEST POSITIVE ( 3 FDA reports)
STRABISMUS ( 3 FDA reports)
STRESS SYMPTOMS ( 3 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 3 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 3 FDA reports)
TENDON PAIN ( 3 FDA reports)
TESTICULAR PAIN ( 3 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 3 FDA reports)
THYROID CYST ( 3 FDA reports)
THYROTOXIC CRISIS ( 3 FDA reports)
TINEA PEDIS ( 3 FDA reports)
TONGUE INJURY ( 3 FDA reports)
TONSILLECTOMY ( 3 FDA reports)
TOXIC NEUROPATHY ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TRANCE ( 3 FDA reports)
TRAUMATIC FRACTURE ( 3 FDA reports)
TRAUMATIC INTRACRANIAL HAEMORRHAGE ( 3 FDA reports)
TRIPLE VESSEL BYPASS GRAFT ( 3 FDA reports)
TUBERCULIN TEST POSITIVE ( 3 FDA reports)
TUMOUR EXCISION ( 3 FDA reports)
ULNAR NERVE INJURY ( 3 FDA reports)
UNEXPECTED THERAPEUTIC DRUG EFFECT ( 3 FDA reports)
UNINTENDED PREGNANCY ( 3 FDA reports)
URETHRAL HAEMORRHAGE ( 3 FDA reports)
URINE SODIUM INCREASED ( 3 FDA reports)
UTERINE ATROPHY ( 3 FDA reports)
UVEITIS ( 3 FDA reports)
VAGINAL LESION ( 3 FDA reports)
VANISHING BILE DUCT SYNDROME ( 3 FDA reports)
VARICOSE ULCERATION ( 3 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 3 FDA reports)
VENOOCCLUSIVE DISEASE ( 3 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 3 FDA reports)
VIRAL LOAD INCREASED ( 3 FDA reports)
VISUAL PATHWAY DISORDER ( 3 FDA reports)
VITAMIN B12 DECREASED ( 3 FDA reports)
VITAMIN K INCREASED ( 3 FDA reports)
VITILIGO ( 3 FDA reports)
VOCAL CORD INFLAMMATION ( 3 FDA reports)
VOLUME BLOOD DECREASED ( 3 FDA reports)
VULVECTOMY ( 3 FDA reports)
VULVOVAGINAL DRYNESS ( 3 FDA reports)
WAIST CIRCUMFERENCE INCREASED ( 3 FDA reports)
ABDOMINAL SEPSIS ( 3 FDA reports)
ABDOMINAL WALL ABSCESS ( 3 FDA reports)
ABORTION ( 3 FDA reports)
ACCIDENTAL NEEDLE STICK ( 3 FDA reports)
ACQUIRED HAEMOPHILIA ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 3 FDA reports)
ADRENAL SUPPRESSION ( 3 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 3 FDA reports)
AGITATION POSTOPERATIVE ( 3 FDA reports)
AGNOSIA ( 3 FDA reports)
ALKALOSIS ( 3 FDA reports)
AMAUROSIS FUGAX ( 3 FDA reports)
AMYLASE INCREASED ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 3 FDA reports)
ANAL FISTULA ( 3 FDA reports)
ANASTOMOTIC ULCER ( 3 FDA reports)
ANGIOGRAM ABNORMAL ( 3 FDA reports)
ANTICOAGULATION DRUG LEVEL ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL ABNORMAL ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 3 FDA reports)
AORTIC VALVE DISEASE MIXED ( 3 FDA reports)
APLASIA ( 3 FDA reports)
APPLICATION SITE BLEEDING ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
APTYALISM ( 3 FDA reports)
ARTERIOGRAM CORONARY ( 3 FDA reports)
ARTERIOVENOUS FISTULA ( 3 FDA reports)
ASBESTOSIS ( 3 FDA reports)
ASPIRATION BONE MARROW ( 3 FDA reports)
ASTHMATIC CRISIS ( 3 FDA reports)
ATRIAL PRESSURE INCREASED ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 3 FDA reports)
BACILLUS INFECTION ( 3 FDA reports)
BACTERIA URINE ( 3 FDA reports)
BACTERIURIA ( 3 FDA reports)
BALLISMUS ( 3 FDA reports)
BENIGN BREAST NEOPLASM ( 3 FDA reports)
BENIGN GASTROINTESTINAL NEOPLASM ( 3 FDA reports)
BETA 2 MICROGLOBULIN INCREASED ( 3 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 3 FDA reports)
BILIARY CIRRHOSIS ( 3 FDA reports)
BILIARY TRACT INFECTION ( 3 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 3 FDA reports)
BIOPSY KIDNEY ( 3 FDA reports)
BIOPSY KIDNEY ABNORMAL ( 3 FDA reports)
BLADDER CYST ( 3 FDA reports)
BLEEDING TIME SHORTENED ( 3 FDA reports)
BLEEDING VARICOSE VEIN ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 3 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 3 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 3 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 3 FDA reports)
BLOOD PROLACTIN INCREASED ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE ABNORMAL ( 3 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 3 FDA reports)
BODY DYSMORPHIC DISORDER ( 3 FDA reports)
BODY FAT DISORDER ( 3 FDA reports)
BONE MARROW OEDEMA ( 3 FDA reports)
BRAIN STEM THROMBOSIS ( 3 FDA reports)
BREAST CANCER IN SITU ( 3 FDA reports)
BREAST INDURATION ( 3 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 3 FDA reports)
BRONCHIAL INFECTION ( 3 FDA reports)
BRONCHIAL WALL THICKENING ( 3 FDA reports)
BRUNNER'S GLAND HYPERPLASIA ( 3 FDA reports)
BURN OESOPHAGEAL ( 3 FDA reports)
BUTTERFLY RASH ( 3 FDA reports)
CARCINOEMBRYONIC ANTIGEN INCREASED ( 3 FDA reports)
CARCINOMA ( 3 FDA reports)
CARDIAC INFECTION ( 3 FDA reports)
CARDIAC NEOPLASM UNSPECIFIED ( 3 FDA reports)
CARDIAC PERFORATION ( 3 FDA reports)
CARDIAC STRESS TEST ( 3 FDA reports)
CATARACT SUBCAPSULAR ( 3 FDA reports)
CD4/CD8 RATIO DECREASED ( 3 FDA reports)
CD8 LYMPHOCYTES DECREASED ( 3 FDA reports)
CENTRAL NERVOUS SYSTEM HAEMORRHAGE ( 3 FDA reports)
CEREBELLAR HAEMATOMA ( 3 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 3 FDA reports)
CEREBRAL CYST ( 3 FDA reports)
CEREBRAL HYPERPERFUSION SYNDROME ( 3 FDA reports)
CERVICAL CYST ( 3 FDA reports)
CERVICAL DYSPLASIA ( 3 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 3 FDA reports)
CERVIX CARCINOMA ( 3 FDA reports)
CHEMOTHERAPY ( 3 FDA reports)
CHEST INJURY ( 3 FDA reports)
CHOLANGITIS ACUTE ( 3 FDA reports)
CHONDROMALACIA ( 3 FDA reports)
CHRONIC HEPATITIS ( 3 FDA reports)
CLAUSTROPHOBIA ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 3 FDA reports)
COAGULATION FACTOR DECREASED ( 3 FDA reports)
COLON NEOPLASM ( 3 FDA reports)
COLONIC HAEMORRHAGE ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 3 FDA reports)
CONFABULATION ( 3 FDA reports)
CONFUSION POSTOPERATIVE ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
CONGENITAL HYDROCEPHALUS ( 3 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 3 FDA reports)
CONTACT STOMATITIS ( 3 FDA reports)
CORNEAL DEGENERATION ( 3 FDA reports)
CORNEAL EROSION ( 3 FDA reports)
CORNEAL OEDEMA ( 3 FDA reports)
CORNEAL OPACITY ( 3 FDA reports)
CORONARY ARTERY ANEURYSM ( 3 FDA reports)
CORONARY ARTERY EMBOLISM ( 3 FDA reports)
CRANIAL NEUROPATHY ( 3 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 3 FDA reports)
CULTURE POSITIVE ( 3 FDA reports)
CUSHING'S SYNDROME ( 3 FDA reports)
CYSTITIS BACTERIAL ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DEFAECATION URGENCY ( 3 FDA reports)
DELAYED SLEEP PHASE ( 3 FDA reports)
DENTAL NECROSIS ( 3 FDA reports)
DEPERSONALISATION ( 3 FDA reports)
DIABETIC FOOT ( 3 FDA reports)
DIABETIC GASTROPARESIS ( 3 FDA reports)
DIARRHOEA INFECTIOUS ( 3 FDA reports)
DIPLEGIA ( 3 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 3 FDA reports)
DRUG THERAPEUTIC INCOMPATIBILITY ( 3 FDA reports)
DRY GANGRENE ( 3 FDA reports)
DUODENAL OBSTRUCTION ( 3 FDA reports)
DYSPLASIA ( 3 FDA reports)
DYSTROPHIC CALCIFICATION ( 3 FDA reports)
EAR INFECTION FUNGAL ( 3 FDA reports)
EAR OPERATION ( 3 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
EJACULATION DISORDER ( 3 FDA reports)
EJACULATION FAILURE ( 3 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 3 FDA reports)
ELECTROCARDIOGRAM PR SHORTENED ( 3 FDA reports)
ELECTROCARDIOGRAM QT INTERVAL ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM R ON T PHENOMENON ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
ENAMEL ANOMALY ( 3 FDA reports)
ENDOCARDIAL FIBROSIS ( 3 FDA reports)
ENDOCARDITIS CANDIDA ( 3 FDA reports)
ENTEROBACTER PNEUMONIA ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 3 FDA reports)
EPICONDYLITIS ( 3 FDA reports)
EPIPHYSEAL DISORDER ( 3 FDA reports)
EPISCLERITIS ( 3 FDA reports)
EXTRADURAL ABSCESS ( 3 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 3 FDA reports)
EXTRAVASATION ( 3 FDA reports)
EYE INJURY ( 3 FDA reports)
EYELIDS PRURITUS ( 3 FDA reports)
EYES SUNKEN ( 3 FDA reports)
FACIAL SPASM ( 3 FDA reports)
FACTOR VIII INHIBITION ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
FEEDING TUBE COMPLICATION ( 3 FDA reports)
FEMALE GENITAL-DIGESTIVE TRACT FISTULA ( 3 FDA reports)
FLOPPY IRIS SYNDROME ( 3 FDA reports)
FOETAL HEART RATE ABNORMAL ( 3 FDA reports)
FOOD CRAVING ( 3 FDA reports)
FOREIGN BODY REACTION ( 3 FDA reports)
FORMICATION ( 3 FDA reports)
FRACTURE DISPLACEMENT ( 3 FDA reports)
FRACTURE OF PENIS ( 3 FDA reports)
FRUSTRATION ( 3 FDA reports)
GAIT SPASTIC ( 3 FDA reports)
GALACTORRHOEA ( 3 FDA reports)
GALLBLADDER OBSTRUCTION ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GASTRIC FISTULA ( 3 FDA reports)
GASTRIC NEOPLASM ( 3 FDA reports)
GASTRIC VARICES HAEMORRHAGE ( 3 FDA reports)
GASTROENTERITIS RADIATION ( 3 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 3 FDA reports)
GASTROINTESTINAL INJURY ( 3 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 3 FDA reports)
GASTROINTESTINAL OEDEMA ( 3 FDA reports)
GASTROINTESTINAL TELANGIECTASIA ( 3 FDA reports)
GENITAL CANDIDIASIS ( 3 FDA reports)
GLOBULINS INCREASED ( 3 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 3 FDA reports)
GLOMERULOSCLEROSIS ( 3 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 3 FDA reports)
GRAFT INFECTION ( 3 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 3 FDA reports)
HAEMATOSPERMIA ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMORRHAGIC HEPATIC CYST ( 3 FDA reports)
HAEMORRHOID OPERATION ( 3 FDA reports)
HANGOVER ( 3 FDA reports)
HEART VALVE CALCIFICATION ( 3 FDA reports)
HEART VALVE INSUFFICIENCY ( 3 FDA reports)
HEART VALVE OPERATION ( 3 FDA reports)
HEAT ILLNESS ( 3 FDA reports)
HEPATIC ADENOMA ( 3 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 3 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 3 FDA reports)
HYDROCELE ( 3 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 3 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 3 FDA reports)
HYPERTHERMIA MALIGNANT ( 3 FDA reports)
HYPOCHROMASIA ( 3 FDA reports)
HYPOMANIA ( 3 FDA reports)
HYPOPNOEA ( 3 FDA reports)
HYPOTENSIVE TRANSFUSION REACTION ( 3 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 3 FDA reports)
ILLUSION ( 3 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 3 FDA reports)
IMMUNOGLOBULINS INCREASED ( 3 FDA reports)
IMPULSE-CONTROL DISORDER ( 3 FDA reports)
INCISION SITE HAEMATOMA ( 3 FDA reports)
INFERIOR VENA CAVA DILATATION ( 3 FDA reports)
INFUSION SITE ABSCESS ( 3 FDA reports)
INFUSION SITE ERYTHEMA ( 3 FDA reports)
INFUSION SITE HAEMATOMA ( 3 FDA reports)
INGROWING NAIL ( 3 FDA reports)
INJECTION SITE PARAESTHESIA ( 3 FDA reports)
INNER EAR DISORDER ( 3 FDA reports)
INSULIN RESISTANCE ( 3 FDA reports)
INTENTION TREMOR ( 3 FDA reports)
INTESTINAL ADHESION LYSIS ( 3 FDA reports)
INTRAOCULAR PRESSURE DECREASED ( 3 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 3 FDA reports)
INTRAVENOUS CATHETER MANAGEMENT ( 3 FDA reports)
INTUSSUSCEPTION ( 3 FDA reports)
ISCHAEMIC LIMB PAIN ( 3 FDA reports)
ISCHAEMIC ULCER ( 3 FDA reports)
JC VIRUS INFECTION ( 3 FDA reports)
JEJUNAL ULCER PERFORATION ( 3 FDA reports)
JOINT FLUID DRAINAGE ( 3 FDA reports)
LABILE HYPERTENSION ( 3 FDA reports)
LARYNGEAL CANCER ( 3 FDA reports)
LARYNGEAL DISORDER ( 3 FDA reports)
LARYNGEAL HAEMATOMA ( 3 FDA reports)
LATEX ALLERGY ( 3 FDA reports)
LAZINESS ( 3 FDA reports)
LICHENIFICATION ( 3 FDA reports)
LICHENOID KERATOSIS ( 3 FDA reports)
LIP DISCOLOURATION ( 3 FDA reports)
LIPOATROPHY ( 3 FDA reports)
LISTERIA SEPSIS ( 3 FDA reports)
LIVING IN RESIDENTIAL INSTITUTION ( 3 FDA reports)
LYME DISEASE ( 3 FDA reports)
LYMPHOCYTE COUNT ( 3 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 3 FDA reports)
MACULAR SCAR ( 3 FDA reports)
MAMMOGRAM ABNORMAL ( 3 FDA reports)
MANTLE CELL LYMPHOMA ( 3 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 3 FDA reports)
MEDIAN NERVE INJURY ( 3 FDA reports)
MEDIASTINAL HAEMATOMA ( 3 FDA reports)
MEDIASTINOSCOPY ( 3 FDA reports)
MEDICAL DEVICE CHANGE ( 3 FDA reports)
MENINGITIS BACTERIAL ( 3 FDA reports)
MENINGOCOCCAL INFECTION ( 3 FDA reports)
MENOPAUSAL SYMPTOMS ( 3 FDA reports)
MENOPAUSE DELAYED ( 3 FDA reports)
MENSTRUAL DISORDER ( 3 FDA reports)
MIGRAINE WITH AURA ( 3 FDA reports)
MITOCHONDRIAL MYOPATHY ( 3 FDA reports)
MIXED CONNECTIVE TISSUE DISEASE ( 3 FDA reports)
MONOCYTE COUNT DECREASED ( 3 FDA reports)
MUCOSAL EROSION ( 3 FDA reports)
MUSCLE SPASTICITY ( 3 FDA reports)
MYELOCYTE COUNT INCREASED ( 3 FDA reports)
MYELOID MATURATION ARREST ( 3 FDA reports)
MYOSCLEROSIS ( 3 FDA reports)
NAIL OPERATION ( 3 FDA reports)
NASAL NEOPLASM ( 3 FDA reports)
NEGATIVE THOUGHTS ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NERVE ROOT LESION ( 3 FDA reports)
NIKOLSKY'S SIGN ( 3 FDA reports)
NOCARDIOSIS ( 3 FDA reports)
NON-SMALL CELL LUNG CANCER RECURRENT ( 3 FDA reports)
NORMAL NEWBORN ( 3 FDA reports)
NUCLEATED RED CELLS ( 3 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 3 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 3 FDA reports)
OESOPHAGEAL ACHALASIA ( 3 FDA reports)
OESOPHAGEAL ADENOCARCINOMA ( 3 FDA reports)
OESOPHAGEAL IRRITATION ( 3 FDA reports)
OESOPHAGEAL PAIN ( 3 FDA reports)
OESOPHAGITIS HAEMORRHAGIC ( 3 FDA reports)
OPPORTUNISTIC INFECTION ( 3 FDA reports)
OPTIC DISC DISORDER ( 3 FDA reports)
ORAL MUCOSAL ERUPTION ( 3 FDA reports)
ORAL TORUS ( 3 FDA reports)
ORBITAL CYST ( 3 FDA reports)
ORCHITIS ( 3 FDA reports)
OVARIAN NEOPLASM ( 3 FDA reports)
OXYGEN SATURATION IMMEASURABLE ( 3 FDA reports)
PAINFUL DEFAECATION ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PALPABLE PURPURA ( 3 FDA reports)
PANNICULITIS ( 3 FDA reports)
PAPILLARY THYROID CANCER ( 3 FDA reports)
PARAPSORIASIS ( 3 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 3 FDA reports)
PECTUS EXCAVATUM ( 3 FDA reports)
PENIS DISORDER ( 3 FDA reports)
PERIANAL ABSCESS ( 3 FDA reports)
PERIODIC LIMB MOVEMENT DISORDER ( 3 FDA reports)
ABDOMINAL HERNIA OBSTRUCTIVE ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 2 FDA reports)
ABDOMINAL OPERATION ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABNORMAL PALMAR/PLANTAR CREASES ( 2 FDA reports)
ACALCULIA ( 2 FDA reports)
ACHLORHYDRIA ( 2 FDA reports)
ACNE PUSTULAR ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 2 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 2 FDA reports)
ACUTE TONSILLITIS ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
AGE INDETERMINATE MYOCARDIAL INFARCTION ( 2 FDA reports)
AGONAL RHYTHM ( 2 FDA reports)
AIDS DEMENTIA COMPLEX ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALBUMIN URINE PRESENT ( 2 FDA reports)
ALCOHOL INTOLERANCE ( 2 FDA reports)
ALCOHOLIC ( 2 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 2 FDA reports)
ALLODYNIA ( 2 FDA reports)
ANAESTHETIC COMPLICATION CARDIAC ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANAPHYLACTOID SHOCK ( 2 FDA reports)
ANAPLASTIC LARGE CELL LYMPHOMA T- AND NULL-CELL TYPES ( 2 FDA reports)
ANASTOMOTIC STENOSIS ( 2 FDA reports)
ANEURYSM REPAIR ( 2 FDA reports)
ANHIDROSIS ( 2 FDA reports)
ANIMAL SCRATCH ( 2 FDA reports)
ANOXIA ( 2 FDA reports)
ANTI FACTOR VIII ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-INSULIN ANTIBODY INCREASED ( 2 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-PLATELET ANTIBODY ( 2 FDA reports)
ANTI-PLATELET ANTIBODY POSITIVE ( 2 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
ANTIBODY TEST POSITIVE ( 2 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 2 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY INCREASED ( 2 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 2 FDA reports)
AORTIC ANEURYSM REPAIR ( 2 FDA reports)
APALLIC SYNDROME ( 2 FDA reports)
APNOEIC ATTACK ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
APPLICATION SITE ATROPHY ( 2 FDA reports)
APPLICATION SITE DISCOMFORT ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
APPLICATION SITE SWELLING ( 2 FDA reports)
APPLICATION SITE ULCER ( 2 FDA reports)
ARACHNOID CYST ( 2 FDA reports)
ARCUS LIPOIDES ( 2 FDA reports)
ARTERIAL INSUFFICIENCY ( 2 FDA reports)
ARTERIAL SPASM ( 2 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE HAEMORRHAGE ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
ASTERIXIS ( 2 FDA reports)
ATOPY ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ACQUIRED ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
ATYPICAL FIBROXANTHOMA ( 2 FDA reports)
AURICULAR PERICHONDRITIS ( 2 FDA reports)
AUTOINFLAMMATORY DISEASE ( 2 FDA reports)
B-CELL LYMPHOMA RECURRENT ( 2 FDA reports)
BALANITIS ( 2 FDA reports)
BENIGN BONE NEOPLASM ( 2 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 2 FDA reports)
BEREAVEMENT ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BILIARY CANCER METASTATIC ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BILIARY NEOPLASM ( 2 FDA reports)
BIOPSY LIVER ( 2 FDA reports)
BIOPSY PERIPHERAL NERVE ( 2 FDA reports)
BIOPSY PROSTATE ( 2 FDA reports)
BLADDER CANCER RECURRENT ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLADDER DISCOMFORT ( 2 FDA reports)
BLADDER DISTENSION ( 2 FDA reports)
BLADDER INJURY ( 2 FDA reports)
BLADDER NECK OBSTRUCTION ( 2 FDA reports)
BLADDER OPERATION ( 2 FDA reports)
BLADDER REPAIR ( 2 FDA reports)
BLADDER TAMPONADE ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLISTER INFECTED ( 2 FDA reports)
BLOOD ALBUMIN ABNORMAL ( 2 FDA reports)
BLOOD ALBUMIN INCREASED ( 2 FDA reports)
BLOOD ALCOHOL INCREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 2 FDA reports)
BLOOD AMYLASE DECREASED ( 2 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 2 FDA reports)
BLOOD ARSENIC INCREASED ( 2 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN DECREASED ( 2 FDA reports)
BLOOD COPPER ABNORMAL ( 2 FDA reports)
BLOOD COPPER INCREASED ( 2 FDA reports)
BLOOD FOLATE DECREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN A DECREASED ( 2 FDA reports)
BLOOD LACTIC ACID DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM ABNORMAL ( 2 FDA reports)
BLOOD PHOSPHORUS ABNORMAL ( 2 FDA reports)
BLOOD PRODUCT TRANSFUSION ( 2 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 2 FDA reports)
BONE FORMATION INCREASED ( 2 FDA reports)
BONE GRAFT ( 2 FDA reports)
BRACHYCEPHALY ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN STEM ISCHAEMIA ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
BREAST DISORDER ( 2 FDA reports)
BREAST LUMP REMOVAL ( 2 FDA reports)
BREAST PROSTHESIS USER ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BRONCHIAL DISORDER ( 2 FDA reports)
BRONCHIAL HAEMORRHAGE ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
BRONCHOSCOPY ABNORMAL ( 2 FDA reports)
BUDD-CHIARI SYNDROME ( 2 FDA reports)
CALCIUM DEFICIENCY ( 2 FDA reports)
CALCULUS BLADDER ( 2 FDA reports)
CANDIDA PNEUMONIA ( 2 FDA reports)
CARCINOID SYNDROME ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARDIAC MYXOMA ( 2 FDA reports)
CARDIAC PSEUDOANEURYSM ( 2 FDA reports)
CARDIAC RESYNCHRONISATION THERAPY ( 2 FDA reports)
CARDIO-RESPIRATORY DISTRESS ( 2 FDA reports)
CARDIOTHORACIC RATIO INCREASED ( 2 FDA reports)
CAST APPLICATION ( 2 FDA reports)
CATAPLEXY ( 2 FDA reports)
CATHETER SITE CELLULITIS ( 2 FDA reports)
CATHETER SITE HAEMATOMA ( 2 FDA reports)
CATHETER SITE OEDEMA ( 2 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CEREBRAL ATHEROSCLEROSIS ( 2 FDA reports)
CEREBRAL ATROPHY CONGENITAL ( 2 FDA reports)
CEREBRAL HYPOPERFUSION ( 2 FDA reports)
CEREBROVASCULAR INSUFFICIENCY ( 2 FDA reports)
CHEMICAL BURN OF SKIN ( 2 FDA reports)
CHOLELITHIASIS OBSTRUCTIVE ( 2 FDA reports)
CHOLURIA ( 2 FDA reports)
CHOREOATHETOSIS ( 2 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CHRONIC HEPATIC FAILURE ( 2 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 2 FDA reports)
COAGULATION FACTOR INCREASED ( 2 FDA reports)
COAGULATION FACTOR V LEVEL ABNORMAL ( 2 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
COLONOSCOPY ABNORMAL ( 2 FDA reports)
COMPLEMENT FACTOR C4 DECREASED ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LIVER ( 2 FDA reports)
COMPULSIVE LIP BITING ( 2 FDA reports)
COMPULSIVE SHOPPING ( 2 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 2 FDA reports)
CONGENITAL ATRIAL SEPTAL DEFECT ( 2 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 2 FDA reports)
CONJUNCTIVAL NEOPLASM ( 2 FDA reports)
CONJUNCTIVAL OEDEMA ( 2 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 2 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 2 FDA reports)
CORNEAL DEPOSITS ( 2 FDA reports)
CORNEAL REFLEX DECREASED ( 2 FDA reports)
CORONARY ARTERY REOCCLUSION ( 2 FDA reports)
CREATINE PHOSPHOKINASE DECREASED ( 2 FDA reports)
CROSS SENSITIVITY REACTION ( 2 FDA reports)
CSF PRESSURE INCREASED ( 2 FDA reports)
CYSTITIS ESCHERICHIA ( 2 FDA reports)
CYSTITIS NONINFECTIVE ( 2 FDA reports)
CYSTITIS RADIATION ( 2 FDA reports)
CYTOGENETIC ABNORMALITY ( 2 FDA reports)
CYTOKINE RELEASE SYNDROME ( 2 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 2 FDA reports)
CYTOMEGALOVIRUS MUCOCUTANEOUS ULCER ( 2 FDA reports)
DEATH NEONATAL ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DEPENDENCE ON RESPIRATOR ( 2 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 2 FDA reports)
DEVICE BREAKAGE ( 2 FDA reports)
DEVICE EXPULSION ( 2 FDA reports)
DEVICE MIGRATION ( 2 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 2 FDA reports)
DIAGNOSTIC PROCEDURE ( 2 FDA reports)
DIAPHRAGMATIC DISORDER ( 2 FDA reports)
DIAPHRAGMATIC PARALYSIS ( 2 FDA reports)
DIASTOLIC HYPERTENSION ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DISLOCATION OF JOINT PROSTHESIS ( 2 FDA reports)
DISORDER OF GLOBE ( 2 FDA reports)
DISSOCIATIVE DISORDER ( 2 FDA reports)
DIVERTICULITIS MECKEL'S ( 2 FDA reports)
DRUG EFFECT PROLONGED ( 2 FDA reports)
DRUG TOLERANCE DECREASED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 2 FDA reports)
DUPUYTREN'S CONTRACTURE ( 2 FDA reports)
DYSLEXIA ( 2 FDA reports)
EJECTION FRACTION ( 2 FDA reports)
ELBOW OPERATION ( 2 FDA reports)
ELECTROCARDIOGRAM AMBULATORY ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE BIPHASIC ( 2 FDA reports)
ELECTROLYTE DEPLETION ( 2 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 2 FDA reports)
ENDOCRINE DISORDER ( 2 FDA reports)
ENDOMETRIAL HYPERTROPHY ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENZYME ABNORMALITY ( 2 FDA reports)
ENZYME INDUCTION ( 2 FDA reports)
EOSINOPHILS URINE PRESENT ( 2 FDA reports)
EPIGLOTTIC OEDEMA ( 2 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 2 FDA reports)
ERECTION INCREASED ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
EXCESSIVE MASTURBATION ( 2 FDA reports)
EXPOSURE TO CHEMICAL POLLUTION ( 2 FDA reports)
EXSANGUINATION ( 2 FDA reports)
EYE ABSCESS ( 2 FDA reports)
EYE OPERATION COMPLICATION ( 2 FDA reports)
EYE PENETRATION ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
EYELID OPERATION ( 2 FDA reports)
FACIAL WASTING ( 2 FDA reports)
FACTOR VIII DEFICIENCY ( 2 FDA reports)
FAECAL DISIMPACTION ( 2 FDA reports)
FAECAL OCCULT BLOOD ( 2 FDA reports)
FAECAL VOLUME DECREASED ( 2 FDA reports)
FAT TISSUE INCREASED ( 2 FDA reports)
FEAR OF WEIGHT GAIN ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
FEEDING DISORDER NEONATAL ( 2 FDA reports)
FEMORAL ARTERY ANEURYSM ( 2 FDA reports)
FEMORAL ARTERY EMBOLISM ( 2 FDA reports)
FLUCTUANCE ( 2 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 2 FDA reports)
FOETAL DAMAGE ( 2 FDA reports)
FOETAL GROWTH RETARDATION ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOD POISONING ( 2 FDA reports)
FREEZING PHENOMENON ( 2 FDA reports)
GALLBLADDER INJURY ( 2 FDA reports)
GASTRIC INFECTION ( 2 FDA reports)
GASTRIC MUCOSAL HYPERTROPHY ( 2 FDA reports)
GASTRITIS BACTERIAL ( 2 FDA reports)
GASTRODUODENAL HAEMORRHAGE ( 2 FDA reports)
GASTROENTERITIS ESCHERICHIA COLI ( 2 FDA reports)
GASTROINTESTINAL ANGIODYSPLASIA HAEMORRHAGIC ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GASTROINTESTINAL VASCULAR MALFORMATION ( 2 FDA reports)
GENERAL ANAESTHESIA ( 2 FDA reports)
GENERAL SYMPTOM ( 2 FDA reports)
GENITAL PRURITUS FEMALE ( 2 FDA reports)
GERSTMANN'S SYNDROME ( 2 FDA reports)
GESTATIONAL DIABETES ( 2 FDA reports)
GINGIVAL EROSION ( 2 FDA reports)
GLIOBLASTOMA MULTIFORME ( 2 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 2 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 2 FDA reports)
GLOMERULONEPHROPATHY ( 2 FDA reports)
GRAFT COMPLICATION ( 2 FDA reports)
GRAFT THROMBOSIS ( 2 FDA reports)
GRAVITATIONAL OEDEMA ( 2 FDA reports)
GRUNTING ( 2 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 2 FDA reports)
HAEMATOPOIETIC NEOPLASM ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HAEMODILUTION ( 2 FDA reports)
HAEMORRHAGE SUBEPIDERMAL ( 2 FDA reports)
HAEMORRHAGIC ARTERIOVENOUS MALFORMATION ( 2 FDA reports)
HAND AMPUTATION ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HAPTOGLOBIN INCREASED ( 2 FDA reports)
HEART BLOCK CONGENITAL ( 2 FDA reports)
HEART TRANSPLANT REJECTION ( 2 FDA reports)
HEPAPLASTIN DECREASED ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA TEST POSITIVE ( 2 FDA reports)
HEPATIC CANCER METASTATIC ( 2 FDA reports)
HEPATIC HYDROTHORAX ( 2 FDA reports)
HEPATIC VEIN THROMBOSIS ( 2 FDA reports)
HERNIA OBSTRUCTIVE ( 2 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 2 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 2 FDA reports)
HIV INFECTION ( 2 FDA reports)
HORMONE LEVEL ABNORMAL ( 2 FDA reports)
HUNTINGTON'S DISEASE ( 2 FDA reports)
HYPERADRENOCORTICISM ( 2 FDA reports)
HYPERAEMIA ( 2 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 2 FDA reports)
HYPERGLOBULINAEMIA ( 2 FDA reports)
HYPERLIPASAEMIA ( 2 FDA reports)
HYPEROSMOLAR STATE ( 2 FDA reports)
HYPERSEXUALITY ( 2 FDA reports)
HYPERTELORISM OF ORBIT ( 2 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPERTROPHIC OSTEOARTHROPATHY ( 2 FDA reports)
HYPERTROPHY BREAST ( 2 FDA reports)
HYPOGLYCAEMIC ENCEPHALOPATHY ( 2 FDA reports)
HYPOPARATHYROIDISM ( 2 FDA reports)
HYPOSMIA ( 2 FDA reports)
ICHTHYOSIS ACQUIRED ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
ILEAL STENOSIS ( 2 FDA reports)
ILEAL ULCER ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
ILIAC VEIN OCCLUSION ( 2 FDA reports)
IMPAIRED FASTING GLUCOSE ( 2 FDA reports)
IMPLANT SITE PAIN ( 2 FDA reports)
IMPLANT SITE REACTION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR MALFUNCTION ( 2 FDA reports)
IMPLANTABLE DEFIBRILLATOR REMOVAL ( 2 FDA reports)
IMPULSIVE BEHAVIOUR ( 2 FDA reports)
IN-STENT ARTERIAL RESTENOSIS ( 2 FDA reports)
INDIFFERENCE ( 2 FDA reports)
INFECTED DERMAL CYST ( 2 FDA reports)
INFECTED INSECT BITE ( 2 FDA reports)
INFLAMMATION OF WOUND ( 2 FDA reports)
INFLAMMATORY MARKER INCREASED ( 2 FDA reports)
INFREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
INFUSION SITE EXTRAVASATION ( 2 FDA reports)
INFUSION SITE NECROSIS ( 2 FDA reports)
INFUSION SITE PHLEBITIS ( 2 FDA reports)
INFUSION SITE REACTION ( 2 FDA reports)
INFUSION SITE SWELLING ( 2 FDA reports)
INFUSION SITE THROMBOSIS ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE INJURY ( 2 FDA reports)
INJECTION SITE PAPULE ( 2 FDA reports)
INJECTION SITE THROMBOSIS ( 2 FDA reports)
INJECTION SITE ULCER ( 2 FDA reports)
INJECTION SITE VESICLES ( 2 FDA reports)
INSULIN AUTOIMMUNE SYNDROME ( 2 FDA reports)
INSULIN C-PEPTIDE INCREASED ( 2 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
INTERCAPILLARY GLOMERULOSCLEROSIS ( 2 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 2 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 2 FDA reports)
INTESTINAL ANASTOMOSIS COMPLICATION ( 2 FDA reports)
INTESTINAL GANGRENE ( 2 FDA reports)
INTESTINAL MALROTATION ( 2 FDA reports)
INTUBATION COMPLICATION ( 2 FDA reports)
INVESTIGATION ABNORMAL ( 2 FDA reports)
IRON OVERLOAD ( 2 FDA reports)
JAUNDICE ACHOLURIC ( 2 FDA reports)
KERATITIS HERPETIC ( 2 FDA reports)
KERATOACANTHOMA ( 2 FDA reports)
KLEPTOMANIA ( 2 FDA reports)
LABELLED DRUG-FOOD INTERACTION MEDICATION ERROR ( 2 FDA reports)
LACRIMAL DISORDER ( 2 FDA reports)
LACTOBACILLUS INFECTION ( 2 FDA reports)
LARYNGEAL MASS ( 2 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 2 FDA reports)
LEIOMYOMA ( 2 FDA reports)
LEUKAEMOID REACTION ( 2 FDA reports)
LEUKOARAIOSIS ( 2 FDA reports)
LINEAR IGA DISEASE ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LIP INJURY ( 2 FDA reports)
LIPOSARCOMA METASTATIC ( 2 FDA reports)
LIQUID PRODUCT PHYSICAL ISSUE ( 2 FDA reports)
LISTERIOSIS ( 2 FDA reports)
LOCALISED OSTEOARTHRITIS ( 2 FDA reports)
LOWER LIMB DEFORMITY ( 2 FDA reports)
LUNG CREPITATION ( 2 FDA reports)
LUNG OPERATION ( 2 FDA reports)
LUPUS NEPHRITIS ( 2 FDA reports)
LYMPH NODE TUBERCULOSIS ( 2 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 2 FDA reports)
LYMPHANGITIS ( 2 FDA reports)
MACULAR HOLE ( 2 FDA reports)
MACULE ( 2 FDA reports)
MAGNESIUM METABOLISM DISORDER ( 2 FDA reports)
MALIGNANT HEPATOBILIARY NEOPLASM ( 2 FDA reports)
MALIGNANT NEOPLASM OF CORNEA ( 2 FDA reports)
MALIGNANT SPLENIC NEOPLASM ( 2 FDA reports)
MAMMOGRAM ( 2 FDA reports)
MANDIBULECTOMY ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MEDICAL DEVICE IMPLANTATION ( 2 FDA reports)
MELANOSIS COLI ( 2 FDA reports)
MENINGITIS COCCIDIOIDES ( 2 FDA reports)
MENINGOCOCCAL SEPSIS ( 2 FDA reports)
MENISCUS OPERATION ( 2 FDA reports)
MENOMETRORRHAGIA ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
METAPHYSEAL DYSPLASIA ( 2 FDA reports)
METASTASES TO NASAL SINUSES ( 2 FDA reports)
METHAEMOGLOBINAEMIA ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MINERAL SUPPLEMENTATION ( 2 FDA reports)
MITRAL VALVE SCLEROSIS ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MORAXELLA INFECTION ( 2 FDA reports)
MORPHOEA ( 2 FDA reports)
MOUNTAIN SICKNESS ACUTE ( 2 FDA reports)
MUCOPOLYSACCHARIDOSIS VI ( 2 FDA reports)
MUCOSAL DRYNESS ( 2 FDA reports)
MUSCLE MASS ( 2 FDA reports)
MUSCLE REATTACHMENT ( 2 FDA reports)
MYASTHENIA GRAVIS CRISIS ( 2 FDA reports)
MYCOBACTERIUM CHELONAE INFECTION ( 2 FDA reports)
MYELOFIBROSIS ( 2 FDA reports)
MYELOPATHY ( 2 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 2 FDA reports)
MYOCARDIAL RUPTURE ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
MYOFASCITIS ( 2 FDA reports)
MYRINGITIS ( 2 FDA reports)
NAIL GROWTH ABNORMAL ( 2 FDA reports)
NAIL HYPERTROPHY ( 2 FDA reports)
NASAL INFLAMMATION ( 2 FDA reports)
NASOPHARYNGEAL CANCER ( 2 FDA reports)
NASOPHARYNGEAL DISORDER ( 2 FDA reports)
NECK DEFORMITY ( 2 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 2 FDA reports)
NELSON'S SYNDROME ( 2 FDA reports)
NEONATAL ASPHYXIA ( 2 FDA reports)
NERVE STIMULATION TEST ABNORMAL ( 2 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NEUROSURGERY ( 2 FDA reports)
NEUTROPHIL COUNT ( 2 FDA reports)
NEUTROPHILIC PANNICULITIS ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NITRITE URINE PRESENT ( 2 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OCULOGYRATION ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
OESOPHAGOSCOPY ABNORMAL ( 2 FDA reports)
OLIGODIPSIA ( 2 FDA reports)
OMENTUM NEOPLASM ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
OPTIC DISC HAEMORRHAGE ( 2 FDA reports)
ORAL MUCOSAL DISORDER ( 2 FDA reports)
ORAL NEOPLASM ( 2 FDA reports)
OTITIS MEDIA CHRONIC ( 2 FDA reports)
OVARIAN DISORDER ( 2 FDA reports)
OXYGEN CONSUMPTION DECREASED ( 2 FDA reports)
PACEMAKER GENERATED RHYTHM ( 2 FDA reports)
PANCREATIC ATROPHY ( 2 FDA reports)
PANCREATIC ENLARGEMENT ( 2 FDA reports)
PANCREATIC INSUFFICIENCY ( 2 FDA reports)
PANCREATIC MASS ( 2 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 2 FDA reports)
PANCREATITIS RELAPSING ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PARASPINAL ABSCESS ( 2 FDA reports)
PARATHYROID DISORDER ( 2 FDA reports)
PARVOVIRUS B19 SEROLOGY POSITIVE ( 2 FDA reports)
PAST-POINTING ( 2 FDA reports)
PEDAL PULSE ABSENT ( 2 FDA reports)
PEDAL PULSE DECREASED ( 2 FDA reports)
PELVIC HAEMORRHAGE ( 2 FDA reports)
PERCUTANEOUS CORONARY INTERVENTION ( 2 FDA reports)
PERFORATED ULCER ( 2 FDA reports)
PERIANAL ERYTHEMA ( 2 FDA reports)
PERICARDIAL CALCIFICATION ( 2 FDA reports)
PERICARDIAL DISEASE ( 2 FDA reports)
PERICARDIAL EXCISION ( 2 FDA reports)
PERIODONTAL INFECTION ( 2 FDA reports)
PERIPHERAL NERVOUS SYSTEM NEOPLASM ( 2 FDA reports)
PERIRENAL HAEMATOMA ( 2 FDA reports)
PERITONEAL DIALYSIS COMPLICATION ( 2 FDA reports)
PERITONEAL TUBERCULOSIS ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL INFLAMMATION ( 2 FDA reports)
PHARYNGOTONSILLITIS ( 2 FDA reports)
PHLEBOLITH ( 2 FDA reports)
PHONOPHOBIA ( 2 FDA reports)
PICKWICKIAN SYNDROME ( 2 FDA reports)
PITUITARY HAEMORRHAGE ( 2 FDA reports)
PLACENTAL INSUFFICIENCY ( 2 FDA reports)
PLASMAPHERESIS ( 2 FDA reports)
PLATELET DESTRUCTION INCREASED ( 2 FDA reports)
PLEURAL ADHESION ( 2 FDA reports)
PLEURAL RUB ( 2 FDA reports)
PLEUROTHOTONUS ( 2 FDA reports)
PNEUMATOSIS ( 2 FDA reports)
PNEUMOCOCCAL SEPSIS ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 2 FDA reports)
POISONING DELIBERATE ( 2 FDA reports)
POLYDACTYLY ( 2 FDA reports)
POLYP COLORECTAL ( 2 FDA reports)
POLYPOIDAL CHOROIDAL VASCULOPATHY ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
POST LAMINECTOMY SYNDROME ( 2 FDA reports)
POST PROCEDURAL DRAINAGE ( 2 FDA reports)
POST PROCEDURAL OEDEMA ( 2 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
POST VIRAL FATIGUE SYNDROME ( 2 FDA reports)
POST-TRAUMATIC OSTEOPOROSIS ( 2 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 2 FDA reports)
POSTOPERATIVE FEVER ( 2 FDA reports)
POSTOPERATIVE RESPIRATORY DISTRESS ( 2 FDA reports)
POSTOPERATIVE THORACIC PROCEDURE COMPLICATION ( 2 FDA reports)
PRECIPITATE LABOUR ( 2 FDA reports)
PREGNANCY TEST POSITIVE ( 2 FDA reports)
PRESBYOESOPHAGUS ( 2 FDA reports)
PRODUCT CONTAINER ISSUE ( 2 FDA reports)
PRODUCT CONTAMINATION ( 2 FDA reports)
PRODUCT FORMULATION ISSUE ( 2 FDA reports)
PRODUCT LABEL ISSUE ( 2 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROSTATIC ADENOMA ( 2 FDA reports)
PROSTATIC OBSTRUCTION ( 2 FDA reports)
PSEUDOALDOSTERONISM ( 2 FDA reports)
PSOAS ABSCESS ( 2 FDA reports)
PSYCHOLOGICAL TRAUMA ( 2 FDA reports)
PSYCHOMOTOR RETARDATION ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
PULMONARY COCCIDIOIDES ( 2 FDA reports)
PULMONARY HYPERTENSIVE CRISIS ( 2 FDA reports)
PULMONARY VEIN STENOSIS ( 2 FDA reports)
PULMONARY VENOUS THROMBOSIS ( 2 FDA reports)
PULPITIS DENTAL ( 2 FDA reports)
PURPURA FULMINANS ( 2 FDA reports)
PYLORIC STENOSIS ( 2 FDA reports)
PYRUVATE KINASE INCREASED ( 2 FDA reports)
RADICULITIS ( 2 FDA reports)
RADICULITIS LUMBOSACRAL ( 2 FDA reports)
REBOUND EFFECT ( 2 FDA reports)
RECTAL FISSURE ( 2 FDA reports)
RECTAL TENESMUS ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
REFUSAL OF EXAMINATION ( 2 FDA reports)
REMOVAL OF TRANSPLANTED ORGAN ( 2 FDA reports)
RENAL AMYLOIDOSIS ( 2 FDA reports)
RENAL STONE REMOVAL ( 2 FDA reports)
RENAL TUBERCULOSIS ( 2 FDA reports)
RENAL VESSEL DISORDER ( 2 FDA reports)
REPETITIVE SPEECH ( 2 FDA reports)
RESIDUAL URINE VOLUME ( 2 FDA reports)
RESPIRATORY DYSKINESIA ( 2 FDA reports)
RESPIRATORY TRACT IRRITATION ( 2 FDA reports)
RETINAL ARTERY EMBOLISM ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RETINAL DYSTROPHY ( 2 FDA reports)
RHEUMATOID VASCULITIS ( 2 FDA reports)
SALIVARY GLAND MASS ( 2 FDA reports)
SALPINGO-OOPHORECTOMY BILATERAL ( 2 FDA reports)
SALPINGO-OOPHORITIS ( 2 FDA reports)
SCAN MYOCARDIAL PERFUSION ( 2 FDA reports)
SCAPULA FRACTURE ( 2 FDA reports)
SCHIZOPHRENIA, PARANOID TYPE ( 2 FDA reports)
SCLERODACTYLIA ( 2 FDA reports)
SCROTAL PAIN ( 2 FDA reports)
SEPTIC ARTHRITIS STAPHYLOCOCCAL ( 2 FDA reports)
SERRATIA TEST POSITIVE ( 2 FDA reports)
SERUM SEROTONIN DECREASED ( 2 FDA reports)
SHUNT OCCLUSION ( 2 FDA reports)
SICKLE CELL ANAEMIA ( 2 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 2 FDA reports)
SINUS TARSI SYNDROME ( 2 FDA reports)
SJOGREN'S SYNDROME ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
SKIN DEPIGMENTATION ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SKULL FRACTURED BASE ( 2 FDA reports)
SLEEP ATTACKS ( 2 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 2 FDA reports)
SLEEP TERROR ( 2 FDA reports)
SLOW RESPONSE TO STIMULI ( 2 FDA reports)
SMALL CELL LUNG CANCER METASTATIC ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SODIUM RETENTION ( 2 FDA reports)
SPLENIC EMBOLISM ( 2 FDA reports)
SPLENORENAL SHUNT ( 2 FDA reports)
SPUTUM INCREASED ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
STEAL SYNDROME ( 2 FDA reports)
STOOLS WATERY ( 2 FDA reports)
STREPTOCOCCAL ABSCESS ( 2 FDA reports)
STRESS AT WORK ( 2 FDA reports)
SUBACUTE ENDOCARDITIS ( 2 FDA reports)
SUBDIAPHRAGMATIC ABSCESS ( 2 FDA reports)
SUBDURAL HYGROMA ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUNBURN ( 2 FDA reports)
SUPERFICIAL INJURY OF EYE ( 2 FDA reports)
SURGICAL FAILURE ( 2 FDA reports)
SUSPICIOUSNESS ( 2 FDA reports)
SUTURE REMOVAL ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 2 FDA reports)
SYSTEMIC MYCOSIS ( 2 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
TACHYCARDIA PAROXYSMAL ( 2 FDA reports)
TACHYPHYLAXIS ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
TENOSYNOVITIS ( 2 FDA reports)
TESTIS CANCER ( 2 FDA reports)
THERAPY RESPONDER ( 2 FDA reports)
THROMBOEMBOLECTOMY ( 2 FDA reports)
THROMBOLYSIS ( 2 FDA reports)
THROMBOSIS PROPHYLAXIS ( 2 FDA reports)
TINEA VERSICOLOUR ( 2 FDA reports)
TONGUE BLISTERING ( 2 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 2 FDA reports)
TRACHEAL STENOSIS ( 2 FDA reports)
TRACHEOMALACIA ( 2 FDA reports)
TRANSPLANT ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
TRANSURETHRAL PROSTATECTOMY ( 2 FDA reports)
TRAUMATIC ARTHRITIS ( 2 FDA reports)
TRAUMATIC LIVER INJURY ( 2 FDA reports)
TRICUSPID VALVE REPAIR ( 2 FDA reports)
TROPICAL SPRUE ( 2 FDA reports)
TUBERCULOSIS GASTROINTESTINAL ( 2 FDA reports)
TUBERCULOSIS LIVER ( 2 FDA reports)
TUMOUR FLARE ( 2 FDA reports)
TUMOUR MARKER TEST ( 2 FDA reports)
TUNNEL VISION ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
TYMPANOSCLEROSIS ( 2 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 2 FDA reports)
TYPE V HYPERLIPIDAEMIA ( 2 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 2 FDA reports)
UMBILICAL HERNIA REPAIR ( 2 FDA reports)
UMBILICAL HERNIA, OBSTRUCTIVE ( 2 FDA reports)
UNDERWEIGHT ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINE ARSENIC INCREASED ( 2 FDA reports)
URINE BILIRUBIN INCREASED ( 2 FDA reports)
UROBILIN URINE ( 2 FDA reports)
UROBILIN URINE PRESENT ( 2 FDA reports)
USE OF ACCESSORY RESPIRATORY MUSCLES ( 2 FDA reports)
UTERINE CERVICAL SQUAMOUS METAPLASIA ( 2 FDA reports)
UTERINE DILATION AND CURETTAGE ( 2 FDA reports)
UTERINE NEOPLASM ( 2 FDA reports)
UTERUS EVACUATION ( 2 FDA reports)
VACCINATION COMPLICATION ( 2 FDA reports)
VAGINAL CANCER ( 2 FDA reports)
VAGINAL CANDIDIASIS ( 2 FDA reports)
VAGINAL ULCERATION ( 2 FDA reports)
VASCULAR ACCESS COMPLICATION ( 2 FDA reports)
VASCULAR BYPASS DYSFUNCTION ( 2 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 2 FDA reports)
VASCULAR SHUNT ( 2 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 2 FDA reports)
VEIN PAIN ( 2 FDA reports)
VENOGRAM ( 2 FDA reports)
VENOUS PRESSURE JUGULAR ( 2 FDA reports)
VENOUS STENOSIS ( 2 FDA reports)
VENTRICULAR INTERNAL DIAMETER ABNORMAL ( 2 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 2 FDA reports)
VERTEBRAL INJURY ( 2 FDA reports)
VESTIBULAR ATAXIA ( 2 FDA reports)
VIRAL CARDIOMYOPATHY ( 2 FDA reports)
VIRAL DNA TEST POSITIVE ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
VIRAL SINUSITIS ( 2 FDA reports)
VISUAL ACUITY REDUCED TRANSIENTLY ( 2 FDA reports)
VOCAL CORD THICKENING ( 2 FDA reports)
VULVAL CELLULITIS ( 2 FDA reports)
WEIGHT LOSS POOR ( 2 FDA reports)
WEIL'S DISEASE ( 2 FDA reports)
WOUND DECOMPOSITION ( 2 FDA reports)
X-RAY GASTROINTESTINAL TRACT ABNORMAL ( 2 FDA reports)
XERODERMA ( 2 FDA reports)
PERIPHERAL NERVE OPERATION ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPORTAL SINUS DILATATION ( 1 FDA reports)
PERIPROCTITIS ( 1 FDA reports)
PERITONEAL ADHESIONS ( 1 FDA reports)
PERITONEAL CARCINOMA ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL NEOPLASM ( 1 FDA reports)
PERITONEAL PERFORATION ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PH BODY FLUID ( 1 FDA reports)
PH URINE DECREASED ( 1 FDA reports)
PHAEHYPHOMYCOSIS ( 1 FDA reports)
PHAEOCHROMOCYTOMA ( 1 FDA reports)
PHARYNGEAL CANCER METASTATIC ( 1 FDA reports)
PHARYNGEAL LESION ( 1 FDA reports)
PHARYNGEAL MASS ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHOTOSENSITIVITY ALLERGIC REACTION ( 1 FDA reports)
PHYSICAL ABUSE ( 1 FDA reports)
PINGUECULA ( 1 FDA reports)
PITYRIASIS LICHENOIDES ET VARIOLIFORMIS ACUTA ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLACENTAL DISORDER ( 1 FDA reports)
PLASMINOGEN DECREASED ( 1 FDA reports)
PLATELET AGGREGATION ( 1 FDA reports)
PLATELET AGGREGATION DECREASED ( 1 FDA reports)
PLATELET COUNT ( 1 FDA reports)
PLATELET FUNCTION TEST ABNORMAL ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PLEURAL MESOTHELIOMA MALIGNANT ( 1 FDA reports)
PLEUROPERICARDITIS ( 1 FDA reports)
PNEUMOBILIA ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMOCYSTIS CARINII INFECTION ( 1 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 1 FDA reports)
PNEUMONIA HERPES VIRAL ( 1 FDA reports)
PNEUMONIA MYCOPLASMAL ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
PNEUMOTHORAX TRAUMATIC ( 1 FDA reports)
POIKILODERMA ( 1 FDA reports)
POLYCHONDRITIS ( 1 FDA reports)
POLYCYTHAEMIA VERA ( 1 FDA reports)
POLYMORPHIC LIGHT ERUPTION ( 1 FDA reports)
POLYMYALGIA ( 1 FDA reports)
POLYNEUROPATHY CHRONIC ( 1 FDA reports)
POLYNEUROPATHY IN MALIGNANT DISEASE ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORTAL ANASTOMOSIS ( 1 FDA reports)
PORTAL VEIN FLOW DECREASED ( 1 FDA reports)
PORTAL VEIN PRESSURE INCREASED ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST GASTRIC SURGERY SYNDROME ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POST PROCEDURAL CELLULITIS ( 1 FDA reports)
POST PROCEDURAL HAEMATURIA ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL STROKE ( 1 FDA reports)
POST VACCINATION SYNDROME ( 1 FDA reports)
POST-TRAUMATIC NECK SYNDROME ( 1 FDA reports)
POSTERIOR CAPSULE RUPTURE ( 1 FDA reports)
POSTOPERATIVE HERNIA ( 1 FDA reports)
POSTPARTUM HAEMORRHAGE ( 1 FDA reports)
POSTPARTUM VENOUS THROMBOSIS ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
POUCHITIS ( 1 FDA reports)
POVERTY OF THOUGHT CONTENT ( 1 FDA reports)
PRE-EXISTING DISEASE ( 1 FDA reports)
PREALBUMIN DECREASED ( 1 FDA reports)
PRECANCEROUS SKIN LESION ( 1 FDA reports)
PREGNANCY OF PARTNER ( 1 FDA reports)
PREGNANCY ON CONTRACEPTIVE ( 1 FDA reports)
PREMATURE AGEING ( 1 FDA reports)
PREMATURE EJACULATION ( 1 FDA reports)
PRESBYACUSIS ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PRIMARY IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL VOMITING ( 1 FDA reports)
PROCTOCOLITIS ( 1 FDA reports)
PRODUCT BLISTER PACKAGING ISSUE ( 1 FDA reports)
PRODUCT COUNTERFEIT ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PRODUCT SIZE ISSUE ( 1 FDA reports)
PROSTATE CANCER STAGE III ( 1 FDA reports)
PROSTATIC OPERATION ( 1 FDA reports)
PROTEIN C INCREASED ( 1 FDA reports)
PROTEIN S ABNORMAL ( 1 FDA reports)
PROTEIN S INCREASED ( 1 FDA reports)
PROTEIN TOTAL ABNORMAL ( 1 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 1 FDA reports)
PROTHROMBIN TIME ( 1 FDA reports)
PSEUDOBULBAR PALSY ( 1 FDA reports)
PSEUDOPHAKIA ( 1 FDA reports)
PSEUDOXANTHOMA ELASTICUM ( 1 FDA reports)
PSOAS SIGN ( 1 FDA reports)
PSYCHOSIS POSTOPERATIVE ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY AMYLOIDOSIS ( 1 FDA reports)
PULMONARY ARTERIAL PRESSURE ABNORMAL ( 1 FDA reports)
PULMONARY ARTERY DILATATION ( 1 FDA reports)
PULMONARY CAVITATION ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY HAEMATOMA ( 1 FDA reports)
PULMONARY HILAR ENLARGEMENT ( 1 FDA reports)
PULMONARY MYCOSIS ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULMONARY VASCULAR RESISTANCE ABNORMALITY ( 1 FDA reports)
PUNCTURE SITE DISCHARGE ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PURULENT PERICARDITIS ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYOGENIC GRANULOMA ( 1 FDA reports)
QUADRIPARESIS ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RADIOFREQUENCY ABLATION ( 1 FDA reports)
RASH FOLLICULAR ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
REACTION TO COLOURING ( 1 FDA reports)
REACTION TO PRESERVATIVES ( 1 FDA reports)
RECTAL PERFORATION ( 1 FDA reports)
RED BLOOD CELL AGGLUTINATION ( 1 FDA reports)
RED BLOOD CELL MACROCYTES PRESENT ( 1 FDA reports)
RED BLOOD CELL MORPHOLOGY ABNORMAL ( 1 FDA reports)
RED BLOOD CELL TARGET CELLS PRESENT ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH ABNORMAL ( 1 FDA reports)
RED MAN SYNDROME ( 1 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 1 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA AND RINGED SIDEROBLASTS ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL CANCER METASTATIC ( 1 FDA reports)
RENAL CYST HAEMORRHAGE ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL LYMPHOCELE ( 1 FDA reports)
RENAL OSTEODYSTROPHY ( 1 FDA reports)
REPETITIVE STRAIN INJURY ( 1 FDA reports)
RESIDUAL URINE VOLUME INCREASED ( 1 FDA reports)
RESPIRATORY MONILIASIS ( 1 FDA reports)
RESPITE CARE ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETINAL ANEURYSM ( 1 FDA reports)
RETINAL ARTERY THROMBOSIS ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL PIGMENT EPITHELIOPATHY ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINOPATHY PROLIFERATIVE ( 1 FDA reports)
RETROGRADE EJACULATION ( 1 FDA reports)
RETROGRADE PORTAL VEIN FLOW ( 1 FDA reports)
RIB EXCISION ( 1 FDA reports)
RIFT VALLEY FEVER ( 1 FDA reports)
RUPTURED DIVERTICULUM OF COLON ( 1 FDA reports)
RUSSELL'S VIPER VENOM TIME ABNORMAL ( 1 FDA reports)
SACROILIITIS ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SALMONELLOSIS ( 1 FDA reports)
SALPINGITIS ( 1 FDA reports)
SALPINGO-OOPHORECTOMY ( 1 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 1 FDA reports)
SCIATIC NERVE PALSY ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCLERAL PIGMENTATION ( 1 FDA reports)
SCROTAL HAEMATOCOELE ( 1 FDA reports)
SCROTAL INFECTION ( 1 FDA reports)
SCROTAL VARICOSE VEINS ( 1 FDA reports)
SEBACEOUS CYST EXCISION ( 1 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 1 FDA reports)
SECONDARY AMYLOIDOSIS ( 1 FDA reports)
SECONDARY HYPERTENSION ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SENILE DEMENTIA ( 1 FDA reports)
SEROLOGY ABNORMAL ( 1 FDA reports)
SERUM SEROTONIN INCREASED ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SHUNT ANEURYSM ( 1 FDA reports)
SHUNT STENOSIS ( 1 FDA reports)
SICK RELATIVE ( 1 FDA reports)
SIDEROBLASTIC ANAEMIA ( 1 FDA reports)
SIGMOIDECTOMY ( 1 FDA reports)
SILICON GRANULOMA ( 1 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 1 FDA reports)
SINUS ANTROSTOMY ( 1 FDA reports)
SINUSITIS ASPERGILLUS ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SKIN MACERATION ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SLEEP PARALYSIS ( 1 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 1 FDA reports)
SMALL INTESTINAL STENOSIS ( 1 FDA reports)
SMALL INTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 1 FDA reports)
SMALL INTESTINE ULCER ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SMOOTH MUSCLE ANTIBODY ( 1 FDA reports)
SOFT TISSUE ATROPHY ( 1 FDA reports)
SOLAR URTICARIA ( 1 FDA reports)
SOMATISATION DISORDER ( 1 FDA reports)
SOMATOFORM DISORDER ( 1 FDA reports)
SPECIFIC GRAVITY URINE INCREASED ( 1 FDA reports)
SPERM COUNT DECREASED ( 1 FDA reports)
SPINAL CLAUDICATION ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPINAL CORD INJURY ( 1 FDA reports)
SPINAL CORD ISCHAEMIA ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL FUSION ACQUIRED ( 1 FDA reports)
SPINAL MUSCULAR ATROPHY ( 1 FDA reports)
SPINAL OPERATION ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPLEEN CONGESTION ( 1 FDA reports)
SPLEEN PALPABLE ( 1 FDA reports)
SPLEEN SCAN ABNORMAL ( 1 FDA reports)
SPLENIC CALCIFICATION ( 1 FDA reports)
SPLENIC CYST ( 1 FDA reports)
SPLENIC VEIN OCCLUSION ( 1 FDA reports)
SPLENITIS ( 1 FDA reports)
SPOROTRICHOSIS ( 1 FDA reports)
SPOUSAL ABUSE ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STENOSIS OF VESICOURETHRAL ANASTOMOSIS ( 1 FDA reports)
STENT EMBOLISATION ( 1 FDA reports)
STERNAL INJURY ( 1 FDA reports)
STEROID THERAPY ( 1 FDA reports)
STRAWBERRY TONGUE ( 1 FDA reports)
STREPTOCOCCAL URINARY TRACT INFECTION ( 1 FDA reports)
STRONGYLOIDIASIS ( 1 FDA reports)
SUBCLAVIAN ARTERY STENOSIS ( 1 FDA reports)
SUDDEN VISUAL LOSS ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUPRAVENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SWEAT GLAND INFECTION ( 1 FDA reports)
SYNOVIAL DISORDER ( 1 FDA reports)
SYNOVIAL FLUID CRYSTAL ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
TACHYPHRENIA ( 1 FDA reports)
TANGENTIALITY ( 1 FDA reports)
TANNING ( 1 FDA reports)
TEAR DISCOLOURATION ( 1 FDA reports)
TENDON CALCIFICATION ( 1 FDA reports)
TENODESIS ( 1 FDA reports)
TENONECTOMY ( 1 FDA reports)
TERMINAL INSOMNIA ( 1 FDA reports)
TESTICULAR ABSCESS ( 1 FDA reports)
TESTICULAR ATROPHY ( 1 FDA reports)
THALASSAEMIA ( 1 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THORACIC CAVITY DRAINAGE ( 1 FDA reports)
THROMBECTOMY ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 1 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 1 FDA reports)
THYMIC CANCER METASTATIC ( 1 FDA reports)
THYROXINE INCREASED ( 1 FDA reports)
TILT TABLE TEST ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TONSIL CANCER ( 1 FDA reports)
TONSILLAR HYPERTROPHY ( 1 FDA reports)
TOXIC ANTERIOR SEGMENT SYNDROME ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRABECULECTOMY ( 1 FDA reports)
TRABECULOPLASTY ( 1 FDA reports)
TRACHEAL ULCER ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TREATMENT RELATED SECONDARY MALIGNANCY ( 1 FDA reports)
TREPONEMA TEST POSITIVE ( 1 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 1 FDA reports)
TRICHOMONIASIS ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
TRICUSPID VALVE REPLACEMENT ( 1 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 1 FDA reports)
TRICUSPID VALVE STENOSIS ( 1 FDA reports)
TROUSSEAU'S SYNDROME ( 1 FDA reports)
TUBAL LIGATION ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
TUBO-OVARIAN ABSCESS ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR ULCERATION ( 1 FDA reports)
TYMPANIC MEMBRANE DISORDER ( 1 FDA reports)
TYMPANIC MEMBRANE HYPERAEMIA ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 1 FDA reports)
ULTRASOUND SCAN ABNORMAL ( 1 FDA reports)
UMBILICAL CORD AROUND NECK ( 1 FDA reports)
UMBILICAL CORD VASCULAR DISORDER ( 1 FDA reports)
UPPER LIMB DEFORMITY ( 1 FDA reports)
URATE NEPHROPATHY ( 1 FDA reports)
URETERIC CANCER ( 1 FDA reports)
URETERIC HAEMORRHAGE ( 1 FDA reports)
URETHRAL DILATATION ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URETHRAL STENT INSERTION ( 1 FDA reports)
URINARY BLADDER POLYP ( 1 FDA reports)
URINARY NITROGEN INCREASED ( 1 FDA reports)
URINARY RETENTION POSTOPERATIVE ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
URINE ALBUMIN/CREATININE RATIO INCREASED ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
URINE AMYLASE INCREASED ( 1 FDA reports)
URINE CHLORIDE INCREASED ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE POTASSIUM INCREASED ( 1 FDA reports)
URINOMA ( 1 FDA reports)
UROBILINOGEN URINE INCREASED ( 1 FDA reports)
UROGENITAL HAEMORRHAGE ( 1 FDA reports)
UROSTOMY COMPLICATION ( 1 FDA reports)
UTERINE CERVICAL EROSION ( 1 FDA reports)
UTERINE CERVIX ATROPHY ( 1 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 1 FDA reports)
UTERINE CYST ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
UTERINE HAEMATOMA ( 1 FDA reports)
UTERINE PROLAPSE ( 1 FDA reports)
UVULITIS ( 1 FDA reports)
VAGINAL ERYTHEMA ( 1 FDA reports)
VAGINAL EXFOLIATION ( 1 FDA reports)
VAGINAL LACERATION ( 1 FDA reports)
VASCULAR GRAFT COMPLICATION ( 1 FDA reports)
VASCULAR OPERATION ( 1 FDA reports)
VASCULAR PROCEDURE COMPLICATION ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC INCREASED ( 1 FDA reports)
VASCULITIS GASTROINTESTINAL ( 1 FDA reports)
VASCULITIS NECROTISING ( 1 FDA reports)
VASODILATION PROCEDURE ( 1 FDA reports)
VEILLONELLA TEST POSITIVE ( 1 FDA reports)
VENA CAVA INJURY ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTILATION/PERFUSION SCAN ABNORMAL ( 1 FDA reports)
VENTRICULAR DYSSYNCHRONY ( 1 FDA reports)
VENTRICULAR HYPERKINESIA ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VENTRICULAR WALL THICKENING ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
VESICOURETERIC REFLUX ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VESSEL PUNCTURE SITE BRUISE ( 1 FDA reports)
VICTIM OF CRIME ( 1 FDA reports)
VIRAL PHARYNGITIS ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VIRAL TEST POSITIVE ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN A INCREASED ( 1 FDA reports)
VITAMIN B12 ABNORMAL ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITH NERVE DISORDER ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VITREOUS DISORDER ( 1 FDA reports)
VITRITIS ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VON WILLEBRAND'S DISEASE ( 1 FDA reports)
VON WILLEBRAND'S FACTOR ACTIVITY ABNORMAL ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
VULVITIS ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL ERYTHEMA ( 1 FDA reports)
VULVOVAGINAL PAIN ( 1 FDA reports)
WART EXCISION ( 1 FDA reports)
WEIGHT LOSS DIET ( 1 FDA reports)
WHITE BLOOD CELLS URINE ( 1 FDA reports)
WHITE CLOT SYNDROME ( 1 FDA reports)
WHOLE BLOOD TRANSFUSION ( 1 FDA reports)
WITHDRAWAL OF LIFE SUPPORT ( 1 FDA reports)
WOUND CLOSURE ( 1 FDA reports)
WOUND INFECTION FUNGAL ( 1 FDA reports)
XANTHOMA ( 1 FDA reports)
ZINC DEFICIENCY ( 1 FDA reports)
5'NUCLEOTIDASE INCREASED ( 1 FDA reports)
5Q MINUS SYNDROME ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABNORMAL WEIGHT GAIN ( 1 FDA reports)
ABSCESS FUNGAL ( 1 FDA reports)
ABULIA ( 1 FDA reports)
ACCIDENT AT HOME ( 1 FDA reports)
ACCIDENTAL POISONING ( 1 FDA reports)
ACETONAEMIA ( 1 FDA reports)
ACID-BASE BALANCE DISORDER MIXED ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACINETOBACTER INFECTION ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACQUIRED MACROGLOSSIA ( 1 FDA reports)
ACQUIRED VON WILLEBRAND'S DISEASE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ABNORMAL ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ACUTE STRESS DISORDER ( 1 FDA reports)
ADENOIDECTOMY ( 1 FDA reports)
ADENOMATOUS POLYPOSIS COLI ( 1 FDA reports)
ADHESIOLYSIS ( 1 FDA reports)
ADJUSTMENT DISORDER WITH ANXIETY ( 1 FDA reports)
ADJUSTMENT DISORDER WITH DEPRESSED MOOD ( 1 FDA reports)
ADRENAL CORTEX ATROPHY ( 1 FDA reports)
ADRENAL CORTICAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL HAEMATOMA ( 1 FDA reports)
ADRENOMEGALY ( 1 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 1 FDA reports)
AGONAL DEATH STRUGGLE ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
AIR EMBOLISM ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALCOHOLIC PANCREATITIS ( 1 FDA reports)
ALDOLASE DECREASED ( 1 FDA reports)
ALLERGIC COLITIS ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN DECREASED ( 1 FDA reports)
ALPHA-1 ANTI-TRYPSIN INCREASED ( 1 FDA reports)
ALVEOLITIS FIBROSING ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
AMINO ACID LEVEL INCREASED ( 1 FDA reports)
AMPHETAMINES POSITIVE ( 1 FDA reports)
AMPUTATION STUMP PAIN ( 1 FDA reports)
ANAESTHESIA ( 1 FDA reports)
ANAL ATRESIA ( 1 FDA reports)
ANAL CANDIDIASIS ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANDROGENS DECREASED ( 1 FDA reports)
ANEURYSMECTOMY ( 1 FDA reports)
ANKLE BRACHIAL INDEX DECREASED ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTERIOR CHAMBER DISORDER ( 1 FDA reports)
ANTI-ERYTHROCYTE ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTIBODY TEST NEGATIVE ( 1 FDA reports)
ANTIDEPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 1 FDA reports)
ANTIGLIADIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
ANTITHROMBIN III ( 1 FDA reports)
ANTITHROMBIN III INCREASED ( 1 FDA reports)
AORTIC BRUIT ( 1 FDA reports)
AORTIC BYPASS ( 1 FDA reports)
AORTIC EMBOLUS ( 1 FDA reports)
AORTIC OCCLUSION ( 1 FDA reports)
APPLICATION SITE BURN ( 1 FDA reports)
APPLICATION SITE DRYNESS ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARTERIAL BRUIT ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ARTERIAL REPAIR ( 1 FDA reports)
ARTERIAL STENOSIS LIMB ( 1 FDA reports)
ARTERIOGRAM ABNORMAL ( 1 FDA reports)
ARTERIOGRAM CAROTID ABNORMAL ( 1 FDA reports)
ARTERIOSCLEROTIC RETINOPATHY ( 1 FDA reports)
ARTERIOVENOUS FISTULA, ACQUIRED ( 1 FDA reports)
ARTERIOVENOUS GRAFT ANEURYSM ( 1 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 1 FDA reports)
ARTERIOVENOUS SHUNT OPERATION ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ARTICULAR CALCIFICATION ( 1 FDA reports)
ARTIFICIAL URINARY SPHINCTER IMPLANT ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ASPIRATION JOINT ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
ATHERECTOMY ( 1 FDA reports)
ATHEROSCLEROSIS PROPHYLAXIS ( 1 FDA reports)
ATHETOSIS ( 1 FDA reports)
ATRIOVENTRICULAR DISSOCIATION ( 1 FDA reports)
ATRIOVENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE THROMBOCYTOPENIA ( 1 FDA reports)
AV DISSOCIATION ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTEROIDES BACTERAEMIA ( 1 FDA reports)
BAND NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BASAL GANGLION DEGENERATION ( 1 FDA reports)
BASE EXCESS ( 1 FDA reports)
BASILAR ARTERY THROMBOSIS ( 1 FDA reports)
BASOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BED REST ( 1 FDA reports)
BEHCET'S SYNDROME ( 1 FDA reports)
BENIGN CARDIAC NEOPLASM ( 1 FDA reports)
BENIGN GASTRIC NEOPLASM ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN MIDDLE EAR NEOPLASM ( 1 FDA reports)
BENIGN MUSCLE NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM ( 1 FDA reports)
BENIGN NEOPLASM OF CERVIX UTERI ( 1 FDA reports)
BENIGN NEOPLASM OF PROSTATE ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BENIGN SMALL INTESTINAL NEOPLASM ( 1 FDA reports)
BEREAVEMENT REACTION ( 1 FDA reports)
BETA GLOBULIN DECREASED ( 1 FDA reports)
BIFIDOBACTERIUM TEST POSITIVE ( 1 FDA reports)
BILIARY ANASTOMOSIS COMPLICATION ( 1 FDA reports)
BILIRUBIN URINE ( 1 FDA reports)
BINOCULAR EYE MOVEMENT DISORDER ( 1 FDA reports)
BIOPSY BLADDER ( 1 FDA reports)
BIOPSY PERIPHERAL NERVE ABNORMAL ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BIPOLAR II DISORDER ( 1 FDA reports)
BLADDER DIVERTICULUM ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLAST CELL PROLIFERATION ( 1 FDA reports)
BLEEDING TIME ( 1 FDA reports)
BLEEDING TIME ABNORMAL ( 1 FDA reports)
BLIGHTED OVUM ( 1 FDA reports)
BLOOD CHLORIDE ABNORMAL ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE INCREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD HUMAN CHORIONIC GONADOTROPIN INCREASED ( 1 FDA reports)
BLOOD HYPOSMOSIS ( 1 FDA reports)
BLOOD INSULIN INCREASED ( 1 FDA reports)
BLOOD IRON ABNORMAL ( 1 FDA reports)
BLOOD KETONE BODY INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD METHAEMOGLOBIN PRESENT ( 1 FDA reports)
BLOOD OESTROGEN ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ( 1 FDA reports)
BLOOD PROLACTIN ABNORMAL ( 1 FDA reports)
BLOOD SMEAR TEST ABNORMAL ( 1 FDA reports)
BLOOD THROMBIN DECREASED ( 1 FDA reports)
BLOOD THROMBIN INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URINE ABSENT ( 1 FDA reports)
BODY MASS INDEX DECREASED ( 1 FDA reports)
BODY TINEA ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE INFECTION ( 1 FDA reports)
BONE METABOLISM DISORDER ( 1 FDA reports)
BONE TRIMMING ( 1 FDA reports)
BORRELIA INFECTION ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRACHIAL PLEXUS LESION ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
BRAIN HYPOXIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE DECREASED ( 1 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 1 FDA reports)
BRAIN OPERATION ( 1 FDA reports)
BRAIN STEM STROKE ( 1 FDA reports)
BRANCHIAL CYST ( 1 FDA reports)
BREAST ATROPHY ( 1 FDA reports)
BREAST CANCER STAGE III ( 1 FDA reports)
BREAST CELLULITIS ( 1 FDA reports)
BREAST DISCOLOURATION ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST ENGORGEMENT ( 1 FDA reports)
BREAST INJURY ( 1 FDA reports)
BREAST MICROCALCIFICATION ( 1 FDA reports)
BREAST PROSTHESIS IMPLANTATION ( 1 FDA reports)
BREAST PROSTHESIS REMOVAL ( 1 FDA reports)
BREAST RECONSTRUCTION ( 1 FDA reports)
BREATH SOUNDS ABSENT ( 1 FDA reports)
BREATH SOUNDS DECREASED ( 1 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHIAL IRRITATION ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRONCHITIS VIRAL ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOSPASM PARADOXICAL ( 1 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 1 FDA reports)
BULIMIA NERVOSA ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
BURNS FIRST DEGREE ( 1 FDA reports)
BURSA DISORDER ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
BURSITIS INFECTIVE STAPHYLOCOCCAL ( 1 FDA reports)
CAECITIS ( 1 FDA reports)
CAMPYLOBACTER INTESTINAL INFECTION ( 1 FDA reports)
CANCER IN REMISSION ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CAPILLARY DISORDER ( 1 FDA reports)
CAPILLARY FRAGILITY ( 1 FDA reports)
CAPUT MEDUSAE ( 1 FDA reports)
CARCINOID TUMOUR PULMONARY ( 1 FDA reports)
CARCINOMA IN SITU OF SKIN ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC ANEURYSM REPAIR ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC CIRRHOSIS ( 1 FDA reports)
CARDIAC FUNCTION DISTURBANCE POSTOPERATIVE ( 1 FDA reports)
CARDIAC MALPOSITION ( 1 FDA reports)
CARDIAC PACEMAKER REVISION ( 1 FDA reports)
CARDIAC VALVE PROSTHESIS USER ( 1 FDA reports)
CARDIAC VENTRICULOGRAM LEFT ( 1 FDA reports)
CARDIOLIPIN ANTIBODY ( 1 FDA reports)
CAROTID ANGIOPLASTY ( 1 FDA reports)
CAROTID ARTERY ANEURYSM ( 1 FDA reports)
CAROTID ARTERY DISSECTION ( 1 FDA reports)
CAROTID ARTERY STENT INSERTION ( 1 FDA reports)
CAROTID ARTERY THROMBOSIS ( 1 FDA reports)
CARPAL TUNNEL DECOMPRESSION ( 1 FDA reports)
CATARACT CORTICAL ( 1 FDA reports)
CATHETER SITE INFLAMMATION ( 1 FDA reports)
CATHETER SITE SWELLING ( 1 FDA reports)
CATHETERISATION VENOUS ( 1 FDA reports)
CD4 LYMPHOCYTES ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NECROSIS ( 1 FDA reports)
CEREBRAL AMYLOID ANGIOPATHY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE FOETAL ( 1 FDA reports)
CEREBRAL HAEMORRHAGE NEONATAL ( 1 FDA reports)
CEREBROSCLEROSIS ( 1 FDA reports)
CERUMEN REMOVAL ( 1 FDA reports)
CHEMICAL INJURY ( 1 FDA reports)
CHEMICAL PERITONITIS ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
CHOANAL ATRESIA ( 1 FDA reports)
CHOLEDOCHOENTEROSTOMY ( 1 FDA reports)
CHOLINERGIC SYNDROME ( 1 FDA reports)
CHORDAE TENDINAE RUPTURE ( 1 FDA reports)
CHROMOSOME ABNORMALITY ( 1 FDA reports)
CHRONIC GASTROINTESTINAL BLEEDING ( 1 FDA reports)
CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 1 FDA reports)
CHRONIC RESPIRATORY DISEASE ( 1 FDA reports)
CHRONIC RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
CHYLOTHORAX ( 1 FDA reports)
CIRCULATING ANTICOAGULANT ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
COAGULATION DISORDER NEONATAL ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR XI LEVEL DECREASED ( 1 FDA reports)
COARCTATION OF THE AORTA ( 1 FDA reports)
COCCYDYNIA ( 1 FDA reports)
COITAL BLEEDING ( 1 FDA reports)
COLD EXPOSURE INJURY ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
COLON CANCER STAGE I ( 1 FDA reports)
COLON CANCER STAGE III ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLOSTOMY CLOSURE ( 1 FDA reports)
COMPLEMENT FACTOR C3 DECREASED ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPLICATION OF PREGNANCY ( 1 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 1 FDA reports)
COMPULSIONS ( 1 FDA reports)
CONGENITAL COAGULOPATHY ( 1 FDA reports)
CONGENITAL FOOT MALFORMATION ( 1 FDA reports)
CONGENITAL HERPES SIMPLEX INFECTION ( 1 FDA reports)
CONGENITAL NEUROPATHY ( 1 FDA reports)
CONGENITAL NYSTAGMUS ( 1 FDA reports)
CONGENITAL PHARYNGEAL ANOMALY ( 1 FDA reports)
CONJUNCTIVAL ULCER ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
COOMBS INDIRECT TEST POSITIVE ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORNEAL DECOMPENSATION ( 1 FDA reports)
CORNEAL INFECTION ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
CORONARY ARTERY DILATATION ( 1 FDA reports)
CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
CORONARY REVASCULARISATION ( 1 FDA reports)
CORRECTIVE LENS USER ( 1 FDA reports)
CORTISOL FREE URINE DECREASED ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRANIOTOMY ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CRYOGLOBULINS PRESENT ( 1 FDA reports)
CRYOPYRIN ASSOCIATED PERIODIC SYNDROME ( 1 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 1 FDA reports)
CRYSTAL URINE PRESENT ( 1 FDA reports)
CRYSTALLURIA ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CUTIS LAXA ( 1 FDA reports)
CYANOPSIA ( 1 FDA reports)
CYLINDRURIA ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYST RUPTURE ( 1 FDA reports)
CYSTITIS KLEBSIELLA ( 1 FDA reports)
CYTOGENETIC ANALYSIS ABNORMAL ( 1 FDA reports)
CYTOLOGY ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
DACTYLITIS ( 1 FDA reports)
DARK CIRCLES UNDER EYES ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEAFNESS TRANSITORY ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DELUSION OF REFERENCE ( 1 FDA reports)
DENTAL FISTULA ( 1 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DEPOSIT EYE ( 1 FDA reports)
DEREALISATION ( 1 FDA reports)
DERMATITIS DIAPER ( 1 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 1 FDA reports)
DEVICE CONNECTION ISSUE ( 1 FDA reports)
DEVICE ELECTRICAL FINDING ( 1 FDA reports)
DEVICE INEFFECTIVE ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DEVICE PACING ISSUE ( 1 FDA reports)
DEVICE STIMULATION ISSUE ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETIC ENTEROPATHY ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC GANGRENE ( 1 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIALYSIS DEVICE COMPLICATION ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DIGITAL ULCER ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 1 FDA reports)
DISSEMINATED LARGE CELL LYMPHOMA ( 1 FDA reports)
DISTRACTIBILITY ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DIVERTICULAR FISTULA ( 1 FDA reports)
DROWNING ( 1 FDA reports)
DRUG DELIVERY DEVICE IMPLANTATION ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DIVERSION ( 1 FDA reports)
DRUG EFFECT DELAYED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY ABSENT ( 1 FDA reports)
DRUG TOLERANCE ( 1 FDA reports)
DRUG TOLERANCE INCREASED ( 1 FDA reports)
DUODENAL SPHINCTEROTOMY ( 1 FDA reports)
DUODENOGASTRIC REFLUX ( 1 FDA reports)
DYSAESTHESIA PHARYNX ( 1 FDA reports)
DYSSOMNIA ( 1 FDA reports)
EAR DEFORMITY ACQUIRED ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
EATING DISORDER SYMPTOM ( 1 FDA reports)
ECHOCARDIOGRAM ( 1 FDA reports)
ECTOPIC ACTH SYNDROME ( 1 FDA reports)
ECTOPIC PREGNANCY ( 1 FDA reports)
ECZEMA ASTEATOTIC ( 1 FDA reports)
ECZEMA NUMMULAR ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM LOW VOLTAGE ( 1 FDA reports)
ELECTROCARDIOGRAM PACEMAKER SPIKE ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT DEPRESSION ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
ELECTROOCULOGRAM ABNORMAL ( 1 FDA reports)
ELLIPTOCYTOSIS ( 1 FDA reports)
EMERGENCY CARE EXAMINATION ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ENCHONDROMA ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOCARDITIS ENTEROCOCCAL ( 1 FDA reports)
ENDOCARDITIS FIBROPLASTICA ( 1 FDA reports)
ENDOCARDITIS NONINFECTIVE ( 1 FDA reports)
ENDOLYMPHATIC HYDROPS ( 1 FDA reports)
ENDOMETRIAL ATROPHY ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL CANCER RECURRENT ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE I ( 1 FDA reports)
ENDOMETRIAL CANCER STAGE III ( 1 FDA reports)
ENDOMETRIAL DISORDER ( 1 FDA reports)
ENDOMETRIOSIS ( 1 FDA reports)
ENDOSCOPIC RETROGRADE CHOLANGIOPANCREATOGRAPHY ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
ENDOSCOPY GASTROINTESTINAL ABNORMAL ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EOSINOPHIL COUNT ABNORMAL ( 1 FDA reports)
EOSINOPHILIC CELLULITIS ( 1 FDA reports)
EOSINOPHILIC PUSTULAR FOLLICULITIS ( 1 FDA reports)
EPIDERMOLYSIS ( 1 FDA reports)
EPIGLOTTITIS ( 1 FDA reports)
EPIPLOIC APPENDAGITIS ( 1 FDA reports)
ERDHEIM-CHESTER DISEASE ( 1 FDA reports)
ERYTHEMA NODOSUM LEPROSUM ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EXANTHEMA SUBITUM ( 1 FDA reports)
EXCESSIVE EXERCISE ( 1 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
EXTRUSION OF DEVICE ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
EYE INFECTION BACTERIAL ( 1 FDA reports)
EYEBALL RUPTURE ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELID IRRITATION ( 1 FDA reports)
EYELID PAIN ( 1 FDA reports)
EYELID RETRACTION ( 1 FDA reports)
FABRY'S DISEASE ( 1 FDA reports)
FACTITIOUS DISORDER ( 1 FDA reports)
FACTOR IX DEFICIENCY ( 1 FDA reports)
FACTOR V INHIBITION ( 1 FDA reports)
FACTOR XIII DEFICIENCY ( 1 FDA reports)
FACTOR XIII INHIBITION ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAILED TRIAL OF LABOUR ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FEELINGS OF WORTHLESSNESS ( 1 FDA reports)
FEMORAL BRUIT ( 1 FDA reports)
FEMORAL HERNIA ( 1 FDA reports)
FEMORAL PULSE ABNORMAL ( 1 FDA reports)
FIBROADENOMA OF BREAST ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FOETAL HAEMOGLOBIN ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FOREIGN BODY IN EYE ( 1 FDA reports)
FRACTION OF INSPIRED OXYGEN ( 1 FDA reports)
FRACTURE REDUCTION ( 1 FDA reports)
FRACTURE TREATMENT ( 1 FDA reports)
FRACTURED COCCYX ( 1 FDA reports)
FRIEDREICH'S ATAXIA ( 1 FDA reports)
FRONTAL SINUS OPERATIONS ( 1 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 1 FDA reports)
FULL BLOOD COUNT INCREASED ( 1 FDA reports)
FUMBLING ( 1 FDA reports)
FUNGAL OESOPHAGITIS ( 1 FDA reports)
FUNGATING WOUND ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
FUNGUS URINE TEST POSITIVE ( 1 FDA reports)
GALLBLADDER ABSCESS ( 1 FDA reports)
GALLBLADDER CANCER ( 1 FDA reports)
GALLBLADDER FISTULA ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GALLBLADDER PAIN ( 1 FDA reports)
GAMBLING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC ADENOMA ( 1 FDA reports)
GASTRIC CYST ( 1 FDA reports)
GASTRIC DYSPLASIA ( 1 FDA reports)
GASTRIC LAVAGE ABNORMAL ( 1 FDA reports)
GASTRIC POLYPECTOMY ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROENTERITIS SHIGELLA ( 1 FDA reports)
GASTROENTERITIS STAPHYLOCOCCAL ( 1 FDA reports)
GASTROINTESTINAL STENOSIS ( 1 FDA reports)
GASTROINTESTINAL TRACT ADENOMA ( 1 FDA reports)
GASTROOESOPHAGEAL CANCER ( 1 FDA reports)
GASTROSCHISIS ( 1 FDA reports)
GASTROSTOMY ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
GENERAL NUTRITION DISORDER ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GERM CELL CANCER ( 1 FDA reports)
GINGIVAL ABSCESS ( 1 FDA reports)
GINGIVAL HYPOPLASIA ( 1 FDA reports)
GINGIVECTOMY ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
GLOSSOPHARYNGEAL NERVE DISORDER ( 1 FDA reports)
GONORRHOEA ( 1 FDA reports)
GOUTY TOPHUS ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAFT LOSS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GROIN INFECTION ( 1 FDA reports)
HAEMATOCRIT ( 1 FDA reports)
HAEMATOMYELIA ( 1 FDA reports)
HAEMATURIA TRAUMATIC ( 1 FDA reports)
HAEMODIALYSIS-INDUCED SYMPTOM ( 1 FDA reports)
HAEMODYNAMIC TEST ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHAGIC EROSIVE GASTRITIS ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HAIR DISORDER ( 1 FDA reports)
HAIR DYE USER ( 1 FDA reports)
HALITOSIS ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEAD CIRCUMFERENCE ABNORMAL ( 1 FDA reports)
HEMICEPHALALGIA ( 1 FDA reports)
HEPATIC ARTERY EMBOLISM ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATIC VEIN STENOSIS ( 1 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS ALCOHOLIC ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATITIS C RNA POSITIVE ( 1 FDA reports)
HEPATITIS E ( 1 FDA reports)
HEREDITARY SPHEROCYTOSIS ( 1 FDA reports)
HERNIA HIATUS REPAIR ( 1 FDA reports)
HERPES SIMPLEX OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER OTICUS ( 1 FDA reports)
HERPETIC STOMATITIS ( 1 FDA reports)
HIP SWELLING ( 1 FDA reports)
HIV TEST POSITIVE ( 1 FDA reports)
HODGKIN'S DISEASE MIXED CELLULARITY STAGE UNSPECIFIED ( 1 FDA reports)
HOUSE DUST ALLERGY ( 1 FDA reports)
HTLV-1 ANTIBODY POSITIVE ( 1 FDA reports)
HUMAN ANAPLASMOSIS ( 1 FDA reports)
HUMAN PAPILLOMA VIRUS TEST POSITIVE ( 1 FDA reports)
HYDROCELE MALE INFECTED ( 1 FDA reports)
HYDROPS FOETALIS ( 1 FDA reports)
HYDROTHORAX ( 1 FDA reports)
HYDROXYCORTICOSTEROIDS INCREASED ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERCATABOLISM ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERCREATININAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERGASTRINAEMIA ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPERMOBILITY SYNDROME ( 1 FDA reports)
HYPERPHOSPHATASAEMIA ( 1 FDA reports)
HYPERSPLENISM ( 1 FDA reports)
HYPERTENSIVE EMERGENCY ( 1 FDA reports)
HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA UNAWARENESS ( 1 FDA reports)
HYPOGLYCAEMIC SEIZURE ( 1 FDA reports)
HYPOKALAEMIC SYNDROME ( 1 FDA reports)
HYPOLIPIDAEMIA ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDERS ( 1 FDA reports)
HYPOURICAEMIA ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IIIRD NERVE DISORDER ( 1 FDA reports)
ILEAL PERFORATION ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILIAC VEIN THROMBOSIS ( 1 FDA reports)
IMMOBILISATION PROLONGED ( 1 FDA reports)
IMMUNOGLOBULINS ABNORMAL ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE SWELLING ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INCISION SITE ERYTHEMA ( 1 FDA reports)
INCISION SITE PAIN ( 1 FDA reports)
INCISION SITE PRURITUS ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED BY DEVICE ( 1 FDA reports)
INCORRECT PRODUCT STORAGE ( 1 FDA reports)
INCREASED INSULIN REQUIREMENT ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFECTED SEBACEOUS CYST ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFECTIOUS PLEURAL EFFUSION ( 1 FDA reports)
INFECTIVE TENOSYNOVITIS ( 1 FDA reports)
INFLUENZA IMMUNISATION ( 1 FDA reports)
INFLUENZA SEROLOGY POSITIVE ( 1 FDA reports)
INFUSION SITE BRUISING ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE VESICLES ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INJECTION SITE DISCHARGE ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE PUSTULE ( 1 FDA reports)
INJECTION SITE STINGING ( 1 FDA reports)
INSPIRATORY CAPACITY DECREASED ( 1 FDA reports)
INSULIN-LIKE GROWTH FACTOR INCREASED ( 1 FDA reports)
INTELLIGENCE TEST ABNORMAL ( 1 FDA reports)
INTENSIVE CARE ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERNAL INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO NORMAL ( 1 FDA reports)
INTERTRIGO CANDIDA ( 1 FDA reports)
INTERVERTEBRAL DISC DISPLACEMENT ( 1 FDA reports)
INTERVERTEBRAL DISC OPERATION ( 1 FDA reports)
INTESTINAL ANASTOMOSIS ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE EXPELLED ( 1 FDA reports)
INTRA-UTERINE CONTRACEPTIVE DEVICE REMOVAL ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
INTRASPINAL ABSCESS ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIS ATROPHY ( 1 FDA reports)
IRON BINDING CAPACITY TOTAL DECREASED ( 1 FDA reports)
IRREGULAR SLEEP PHASE ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
ISCHAEMIC NEUROPATHY ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JARISCH-HERXHEIMER REACTION ( 1 FDA reports)
JEALOUS DELUSION ( 1 FDA reports)
JEJUNAL ULCER ( 1 FDA reports)
JOINT ADHESION ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT INJECTION ( 1 FDA reports)
JOINT RECONSTRUCTION ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KAOLIN CEPHALIN CLOTTING TIME PROLONGED ( 1 FDA reports)
KERATITIS FUNGAL ( 1 FDA reports)
KETOACIDOSIS ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
KNEE DEFORMITY ( 1 FDA reports)
KUSSMAUL RESPIRATION ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LACRIMAL GLAND ENLARGEMENT ( 1 FDA reports)
LAPAROTOMY ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LARGE INTESTINAL OBSTRUCTION ( 1 FDA reports)
LARYNGEAL NEOPLASM ( 1 FDA reports)
LDL/HDL RATIO ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE DECREASED ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LEIOMYOSARCOMA ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKAEMIC INFILTRATION ( 1 FDA reports)
LEUKAEMIC INFILTRATION PULMONARY ( 1 FDA reports)
LEUKOPLAKIA ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIGAMENT DISORDER ( 1 FDA reports)
LIGHT CHAIN ANALYSIS DECREASED ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LIMB HYPOPLASIA CONGENITAL ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIPIDS ABNORMAL ( 1 FDA reports)
LIPODYSTROPHY ACQUIRED ( 1 FDA reports)
LIPOGRANULOMA ( 1 FDA reports)
LIPOHYPERTROPHY ( 1 FDA reports)
LIPOMA EXCISION ( 1 FDA reports)
LIPOMATOSIS ( 1 FDA reports)
LIPOMATOUS HYPERTROPHY OF THE INTERATRIAL SEPTUM ( 1 FDA reports)
LIVER CARCINOMA RUPTURED ( 1 FDA reports)
LIVER SARCOIDOSIS ( 1 FDA reports)
LIVER SCAN ABNORMAL ( 1 FDA reports)
LIVIDITY ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LOOSE ASSOCIATIONS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LUNG ADENOCARCINOMA METASTATIC ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE II ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED STAGE IV ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LYMPH NODE CALCIFICATION ( 1 FDA reports)
LYMPH NODE CANCER METASTATIC ( 1 FDA reports)
LYMPHADENITIS BACTERIAL ( 1 FDA reports)
LYMPHATIC DISORDER ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MALIGNANT ATROPHIC PAPULOSIS ( 1 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 1 FDA reports)
MALIGNANT HYPERTENSION ( 1 FDA reports)
MALIGNANT MEDIASTINAL NEOPLASM ( 1 FDA reports)
MALIGNANT NEOPLASM OF ORBIT ( 1 FDA reports)
MALIGNANT RESPIRATORY TRACT NEOPLASM ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MAY-THURNER SYNDROME ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION INCREASED ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MECHANICAL ILEUS ( 1 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 1 FDA reports)
MEDICAL DEVICE REMOVAL ( 1 FDA reports)
MEDICAL DEVICE SITE REACTION ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MEGAKARYOCYTES ABNORMAL ( 1 FDA reports)
MENINGITIS PNEUMOCOCCAL ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MENINGOCELE ( 1 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
MENTAL STATUS CHANGES POSTOPERATIVE ( 1 FDA reports)
MERYCISM ( 1 FDA reports)
MESENTERIC ARTERY STENOSIS ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METAPNEUMOVIRUS INFECTION ( 1 FDA reports)
METASTASES TO BLADDER ( 1 FDA reports)
METASTASES TO HEART ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO NECK ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO SMALL INTESTINE ( 1 FDA reports)
METASTATIC BRONCHIAL CARCINOMA ( 1 FDA reports)
METASTATIC CARCINOID TUMOUR ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MICROBIOLOGY TEST ABNORMAL ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MICROGRAPHIC SKIN SURGERY ( 1 FDA reports)
MICROLITHIASIS ( 1 FDA reports)
MICROSCOPIC POLYANGIITIS ( 1 FDA reports)
MICROVASCULAR ANGINA ( 1 FDA reports)
MIGRAINE WITHOUT AURA ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITOCHONDRIAL MYOPATHY ACQUIRED ( 1 FDA reports)
MITRAL VALVE DISEASE MIXED ( 1 FDA reports)
MONOCYTE COUNT ABNORMAL ( 1 FDA reports)
MONONEUROPATHY ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MORGANELLA TEST POSITIVE ( 1 FDA reports)
MOUTH PLAQUE ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS ( 1 FDA reports)
MUCOSAL ATROPHY ( 1 FDA reports)
MUCOSAL DISCOLOURATION ( 1 FDA reports)
MUCOSAL EXCORIATION ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MULTIPLE ENDOCRINE ADENOMATOSIS TYPE I ( 1 FDA reports)
MULTIPLE SYSTEM ATROPHY ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE ENZYME INCREASED ( 1 FDA reports)
MUTISM ( 1 FDA reports)
MYASTHENIC SYNDROME ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYCOTIC CORNEAL ULCER ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 1 FDA reports)
MYOGLOBINAEMIA ( 1 FDA reports)
NAIL AVULSION ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NAIL PITTING ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NASAL ABSCESS ( 1 FDA reports)
NASAL CAVITY CANCER ( 1 FDA reports)
NASAL CYST ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NASAL OPERATION ( 1 FDA reports)
NASAL SEPTUM ULCERATION ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE STIMULATION TEST NORMAL ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROGLYCOPENIA ( 1 FDA reports)
NEUROPATHIC ARTHROPATHY ( 1 FDA reports)
NEUTROPHIL FUNCTION DISORDER ( 1 FDA reports)
NEUTROPHIL HYPERSEGMENTED MORPHOLOGY PRESENT ( 1 FDA reports)
NIPPLE DISORDER ( 1 FDA reports)
NITRITE URINE ABSENT ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NODULAR REGENERATIVE HYPERPLASIA ( 1 FDA reports)
NON-ALCOHOLIC STEATOHEPATITIS ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER STAGE IV ( 1 FDA reports)
NOSE DEFORMITY ( 1 FDA reports)
OBESITY SURGERY ( 1 FDA reports)
OCCULT BLOOD NEGATIVE ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OCULAR RETROBULBAR HAEMORRHAGE ( 1 FDA reports)
OCULAR TOXICITY ( 1 FDA reports)
OCULOCEPHALOGYRIC REFLEX ABSENT ( 1 FDA reports)
ODDI'S SPHINCTER CONSTRICTION ( 1 FDA reports)
OESOPHAGEAL ADENOCARCINOMA STAGE IV ( 1 FDA reports)
OESOPHAGEAL CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
OESOPHAGEAL NEOPLASM ( 1 FDA reports)
OESOPHAGEAL POLYP ( 1 FDA reports)
OESTRADIOL DECREASED ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
ONYCHALGIA ( 1 FDA reports)
OPEN FRACTURE ( 1 FDA reports)
OPTIC NERVE CUPPING ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
ORF ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OROPHARYNGEAL SPASM ( 1 FDA reports)
OSTEOPETROSIS ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OTOSCOPY ABNORMAL ( 1 FDA reports)
OVERGROWTH BACTERIAL ( 1 FDA reports)
OVERSENSING ( 1 FDA reports)
OVERWORK ( 1 FDA reports)
OXYGEN SATURATION INCREASED ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANCREAS INFECTION ( 1 FDA reports)
PANCREATIC CALCIFICATION ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PARACENTESIS ( 1 FDA reports)
PARADOXICAL DRUG REACTION ( 1 FDA reports)
PARADOXICAL EMBOLISM ( 1 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PARATHYROID GLAND OPERATION ( 1 FDA reports)
PARATRACHEAL LYMPHADENOPATHY ( 1 FDA reports)
PARENTERAL NUTRITION ( 1 FDA reports)
PAROTID GLAND INFLAMMATION ( 1 FDA reports)
PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA ( 1 FDA reports)
PATIENT-DEVICE INCOMPATIBILITY ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PELVIC ADHESIONS ( 1 FDA reports)
PELVIC INFECTION ( 1 FDA reports)
PELVIC INFLAMMATORY DISEASE ( 1 FDA reports)
PELVIC MUSCLES INADEQUATE ( 1 FDA reports)
PELVIC PROLAPSE ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PENILE ABSCESS ( 1 FDA reports)
PENILE INFECTION ( 1 FDA reports)
PENILE OEDEMA ( 1 FDA reports)
PENILE OPERATION ( 1 FDA reports)
PENILE SWELLING ( 1 FDA reports)
PENILE ULCERATION ( 1 FDA reports)
PENIS CARCINOMA ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PERCUSSION TEST ABNORMAL ( 1 FDA reports)
PERICARDIAL DRAINAGE ( 1 FDA reports)
PERIDIVERTICULITIS ( 1 FDA reports)
PERINEPHRIC COLLECTION ( 1 FDA reports)